Bulk Drugs- API-Pharmaceutical Raw Material.

HEPARIN SODIUM IP

HEPARIN SODIUM IP

colchicine USP

COLCHICINE USP COLCHICINE IP COLCHICINE BP

Paprika Oleoresin

1) Capsicum Oleoresin CAS No: 8023-77-6 2) Natural Capsaicin 95 % powder CAS No: 404-86-4 3) Paprika Oleoresin CAS No: 84625-29-6

Capsicum Oleoresin

1. Capsicum Oleoresin CAS No: 8023-77-6 2) Natural Capsaicin 95 % powder CAS No: 404-86-4 3) Paprika Oleoresin CAS No: 84625-29-6

2 .6 Di -picolinic acid

2,6 DIPICOLINIC ACID

ISO Butanol

Iso-Butanol (IBA) is a clear liquid with a characteristic odor. It is miscible with all common solvents. It is obtained in Oxo Synthesis of Propylene (C3H6) and Synthesis gas (H2+CO).

Normal Butanol

Normal Butanol (NBA) is a clear liquid with characteristic odor, miscible in all common solvents. It is produced in OXO synthesis of Propylene (C3H6) and Synthesis gas (H2+CO).

2 Ethyl Hexanol

2-Ethyl Hexanol (2-EH) is a clear high-boiling point and low volatility solvent, uniform, nontoxic liquid with a characteristic odor, insoluble in water, soluble in organic solvent. It is obtained indirectly in OXO synthesis from propylene (C3H6) and synthesis gas (CO + H2) It is also known as Octanol (C8 alcohol)

Manganese Sulphate Solution

Molecular Formula MnSO4 Molecular Weight 151 C.A.S. No. 7732-18-5 Product Group Inorganic Sulphate

Non-ionic flocculants

non-ionic flocculants are water-soluble polymers or polyelectrolytes. Because its molecular chain contains a certain number of polar groups, it can adsorb solid particles suspended in water to bridge between particles or condense particles to form large flocs through charge neutralization.

Dextrose Monohydrate

Dextrose Monohydrate

Sodium benzoate

Sodium Benzoate used as an antifungal preservative in pharmaceutical preparations and foods. It may also be used as a test for liver function Preservative for food and beverages Use as a preservative in pharmaceuticals Agricultural chemicals (non-pesticidal) Corrosion inhibitors and anti-scaling agents Oxidizing/reducing agents Paint additives and coating additives Plating agents and surface treating agents Processing aids Stabilizers

12-HYDROXY STEARIC ACID (12-H.S.A.) FLAKES/ POWDER

2-HSA is a useful component in hot-melt adhesives, inks and polishes, that reacts with acrylic esters to create durable and strong thermosetting polymers. These thermosetting polymers are used as a coating in metal-decorative finishes, industrial appliances and high-quality automotive applications.

Liver Extract Paste

Description: It is an enzymatic digest of Bovine liver of Indian origin. Semi-solid paste with characteristic proteinous odour Application: Source of organic nitrogen recommended in Nutraceutical Formulations especially in Animal Nutrition and Veterinary formulations. Physio-chemical characteristics PARAMETERS STANDARD Colour Chocolate Brown Solubility in water (5% solution) Completely soluble in water Clarity (2% w/v aqueous solution) 100 % Clear solution pH (5 % solution) 6.0 - 7.0 (at room temp.) Total solids NLT 65 % Total nitrogen TN (Kjeldahl Nitrogen) 10.0 - 12.5 % Total protein content 62 to 78 % Vitamin B12 8.2 mcg/gram (on dry basis)

Protein Hydrolysate Paste 65 %

Source Raw Material: Crude Soya protein, Casein(milk) protein, Corn Protein, Collagen Protein Description: It is derived from the enzymatic hydrolysis of desired crude protein further purified to produce concentrated semi-solid Paste with characteristic proteinous odour. Application: It is used in general purpose nutraceutical formulations, agriculture formulations (as Organic Nitrogen) and animal nutritional formulations as a source of hydrolyzed/ digested proteins rich in amino acids and peptides.

Soya Peptone

Description: It is an enzymatic digest of NON GMO defatted Soybean Meal of Indian origin. Free flowing powder with characteristic proteinous odour. Application: Source of organic nitrogen recommended in Culture Media for Analytical microbiology, Diagnostics, Laboratory Reagentand Industrial fermentation.

Collagen Peptide (Regular)

Description: It is an enzymatic hydrolysate of bovine collagen of Indian origin. Raw collagen gets hydrolysed and in turns loses its gelling strength and gives final product which is low in molecular weight and is sparingly soluble in water. It is a free flowing powderwith characteristic proteinous odourand hygroscopic in nature.

Corn Protein Hydrolysate

Corn Protein Hydrolysate is produced by the hydrolysis of the protein extracted from the maize to make a vegetable based bio-nutrient having a good nutritional profile. It is widely used in the pharmaceutical and nutraceutical industries for the production of pills and various types of dietary supplements that are consumed to enhance the metabolism of the body. Corn Protein Hydrolysate can also be used as a flavour enhancer in various in food and beverage industry. It consist of smaller units of amino acids, peptides and many other prime essential nutrients that are easily absorbed by the body

Protein Hydrolysate Liquid 30 %

ource Raw Material: Crude Soya protein, Casein(milk) protein, Corn Protein, Collagen Protein Description: It is derived from the enzymatic hydrolysis of desired crude protein further purified to produce concentrated semi-solid liquid with characteristic proteinous odour. Application: It is used in general purpose nutraceutical formulations, agriculture formulations (as Organic Nitrogen) and animal nutritional formulations as a source of hydrolyzed/ digested proteins rich in amino acids and peptides.

Collagen Hydrolysate

Description: It is an enzymatic hydrolysate of bovine collagen of Indian origin. Raw collagen gets hydrolysed and in turns loses its gelling strength and gives final product which is low in molecular weight and is sparingly soluble in water. It is a free flowing powder with characteristic proteinous odour and hygroscopic in nature. Application: Source of digested/hydrolyzed protein used in Nutraceuticals (Food, Pharma, Diagnostics & Cosmetics)

Soya Protein Hydrolysate

Soya Protein Hydrolysate is a hydrolysed vegetable protein which is produced by boiling the soy within the hydrochloric acid and neutralizing this hot solution with sodium hydroxide. It is similar to the whey protein which is derived from the dairy products. This powdered substance can be mixed with various different liquids to make a thick paste which can be used as a flavour enhancer which can be used in processed foods like soups, chili, sauces, gravies and meat products. Soya Protein Hydrolysate has a good absorption rate due to the smaller size of amino acids and peptides. The chemical breakdown may result in the formation of free glutamines that combines with sodium to form monosodium glutamate.

Meat Extract Paste

Description: It is an enzymatic digest of Bovine Meat of Indian origin. Semi-solid paste with characteristic proteinous odour. Application: Source of organic nitrogen recommended in Nutraceutical Formulations, Analytical microbiology, Diagnostics, Laboratory Reagent and Industrial fermentation. Physio-chemical characteristics PARAMETERS STANDARD Colour Brown Solubility in water (5% solution) Completely soluble in water Clarity (2% w/v aqueous solution) 100 % Clear solution pH (5 % solution) 6.0 - 7.0 (at room temp.) Total solids NLT 65 % Total nitrogen TN (Kjeldahl Nitrogen) 12.5 to 14.2 % (on dry basis) Alpha (Amino Nitrogen) 2.5 to 4 % (on dry basis) Total Ash < 12.0% (on dry basis)

Sodium Carboxy Methyl Cellulose

Sulpho Ortho Anisidine Vinyl Sulphone

Technical Specification SYNONYMS 1-AMINO-2-METHOXY-4-BETA HYDROXY ETHYL SULPHONE SULPHATE ESTER MOLECULAR WEIGHT 311 CAS NO. 26672-22-0 EMPIRICAL FORMULA : C9H13NO7S2 PHYSICAL APPEARANCE : WHITE TO GREY POWDER PURITY (NITRITE VALUE) : 95.00 % MINIMUM PURITY HYDROLYSIS VALUE : 90 % MINIMUM INSOLUBLES IN WATER : <0.50 % MAXIMUM CAPACITY PER ANNUM (IN MTS) 300

4-Hydroxyisoleucine Powder

4-Hydroxyisoleucine Molecular Formula: C6H13NO3 Molecular weight: 147.17232 g/mol

Ferric Isomaltoside IH

Product Name : Ferric Isomaltoside CAS : Molecular Formula : Molecular Weight : Pharmaceutical Grade : IH Therapeutic Category : Hematinic (Intravenous)

Acesulfame potassium

Acesulfame-K

Natural Vitamin E

We are a leading entity, occupied in presenting a wide range of Vitamin E Powder. Furthermore, our customers can avail these products from us at reasonable prices...

Sodium Bicarbonate IP/BP

Sodium Bicarbonate IP/BP

Carrageenan Powder

Carrageenan food is a general name for polysaccharides and is extracted from selected species of red seaweed. Carrageenan is a natural hydrocolloid with unique functionalities, which is ideal for food additives: they have a range of gelling and emulsifying properties

Chicory Extract

Liquid Chicory extract is made by concentrating the slurry obtained by grinding,mixing and heating raw chicory. It contains various soluble fibers that help lower LDL (bad) blood cholesterol by interfering with the absorption of dietary cholesterol.

Beta alanine

Beta alanine powder

Fructos Oligosaccharides

Fructo-oligosaccharides

Pectin Powder

pectin powder used in food and pharma industries buyer can avail these product from us .

Maltitol Powder

Maltitol Powder is a sugar alcohol (a polyol) used as a sugar substitute. Maltitol is a disaccharide produced by hydrogenation of maltose obtained from starch. Maltitol syrup, a hydrogenated starch hydrolysate,

Creapure Powder

Creatine monohydrate is the king of the creatine supplement world. Creatine monohydrate is 88% pure creatine bound with 12% water.

STEVIA 95%

STEVIA 95%

Betacyclodextrin Material

Usage: -Cyclodextrin is a cyclic oligosaccharide produced from starch via enzymatic conversion. -Cyclodextrin is commonly used to produce HPLC columns allowing chiral enantiomers separation

Calcium D Pantothenate

we are the leading supplier of Calcium D-pantothenate.

Pregelatinized Starch

Packaging Size 25Kg Color White Form Powder

Mono Ethylene Glycol

nti-freezing Agents Heat Transferring Agents Laboratory Chemicals Printing Rubber Manufacture Semiconductors Wood Stains and Varnishes aircraft anti-icer and deicers coolants

Glycerine Liquid

plastics & resins Cosmetics Writing dyes and inks Oils and lubricants Adsorbents and absorbents Processing aids razing Paste component for joining carbon and stainless steel components Coatings and/or defoamers Solvent in hard surface cleaners, and disinfectants

Di Methyl Formamide

Acrylic Fiber Manufacture SBR Latex Production manufacturing dyes fertilisers pesticides, and herbicides

Glutaraldehyde 50%

Usage/Application Surface Disinfectant Packaging Size 220 kg drum Packaging Type Drum Grade Commercial Functions Biocides Purity (%) 50%

3-CHLORO SALICYLIC ACID

CAS 1829-32-9 Molecular Formula C7H5ClO3 Molecular Weight] 172.57

3-METHOXY PHENOL

3-Methoxyphenol [CAS] 150-19-6 1-HYDROXY-3-METHOXYBENZENE 3-HYDROXYANISOL 3-HYDROXYANISOLE 3-METHOXYPHENOL M-HYDROXYANISOLE

Sodium Starch Glycolate

Being the sodium salt of carboxymethyl ether, Sodium Starch Glycolate is a white to off-white, odourless, tasteless, free-flowing powder. It is practically insoluble in water and also in most organic solvents. This product is used as a pharmaceutical-grade dissolution agent and super disintegrant which is produced from corn or potato starch. Sodium Starch Glycolate is spherical granules that absorbs water rapidly and swell up. Sodium Starch Glycolate can be added in capsules and tablets to let them dissolve better and making it easier to absorb. PCSPL is manufacturing Sodium Starch Glycolate which is well-suited for use in tablets and capsules, matching all the international standards.

Croscarmellose Sodium

DESCRIPTION Crosslinked Polymer of Carboxy Methyl Cellulose Sodium White Fibrous Powder Odorless Insoluble and Highly absorbent product with good Swelling Properties APPLICATIONS Used as Disintegrant in Capsules, Tablet and Granule Formulations. STORAGE Stored in Well Closed Container at Cool and Dry Place as Croscarmellose Sodium is Hygroscopic by Nature. Packaging & Shipping

Silicified Microcrystalline Cellulose

Silicified Microcrystalline Cellulose USP Solution for Optimum Compatibility Silicification of MCC increased physical properties such as true density, Hausner ratio, porosity, ejection force and specific surface area. Other properties such as bulk and tap densities were reduced due to the amorphous and light character of fumed silica.

Cyclohexanedione material

A key intermediate used to manufacture herbicides and beta blocker drugs. Industry: Crop Protection Chemicals, Pharmaceutical Product group: Intermediates Synonyms: Cyclohexane-1,3-dione; Dihydroresorcin; Dihydroresorcinol; Hydroresorcinol CAS number: 504-02-9

Resorcinol powder

Physical properties Flash point 127C Boiling point 281.4C Density 1.271 g/cm3 at 20C Vapour pressure 0.065 Pa at 20C Ignition temperature 605C Description Resorcinol comes in the form of white to off-white flakes. Applications Intermediate for dyestuffs, personal care products, pharmaceuticals, rubber and tyre industry Packaging Resorcinol is available in 25 kg paper bags and 500 kg jumbo bags. Other packaging may be considered on request.

5-CHLORO SALICYLIC ACID

AS 321-14-2 5-CHLORO SALICYLIC ACID Molecular Formula C7H5ClO3 Molecular Weight 172.57

Lactoferrin Powder

Appearance Light red crystalline powder Storage Cool & Dry Place Purity 99% Form Powder Shelf Life 1 Year Ash Content 1.5% Molecular Weight 3125.8274 Molecular Formula C141H224N46O29S3

Sodium Monochloro Acetate

DESCRIPTION It is derived from Monochloro Acetic Acid by neutralizing with Alkali White Powder Highly Soluble in Water Pungent Odor Highly Hygroscopic in Nature Odorless Hazardous Product Under UN No.2659 Packing Group III, IMCO Class 6.1

Pregelatinized Starch

Pregelatinized starch is Physically modified starch, it is partially soluble in Cold water. Pregelatinized starch is widely used in pharmaceutical because it is bland, odourless and capable of digestion. Pregelatinized Starch swell in cold water and therefore reduce time/cost compared with traditional starch paste preparation. Pregelatinized starch is widely used as a pharmaceutical aid, especially as a filler-binder. Pregelatinized starch greatly endues the compressibility as well as improves the fluidity of the tablets. Pregelatinized Starch, having excellent flow properties and bulk density, allow homogenous filling of capsules. Pregelatinized food starch used as thickening, texturing and stabilizing agent in cream fillings, canned, sauces, soup mixes, gravies, tomato ketchup, pasty creams, dairy desserts and other food product industries.

Magnesium Stearate

Magnesium Stearate is the most commonly used lubricant for tablets. Magnesium Stearate is also useful because it has lubricating properties, preventing ingredients from sticking to manufacturing equipment during the compression of chemical powders into solid tablets. Magnesium Stearate is often used as an anti-adherent in the manufacture of medical tablets, capsules and powder. Magnesium Stearate can also be used efficiently in dry coating processes. e Magnesium Stearate is also used to bind sugar in hard candies like mints, and is acommon ingredient in baby formulas.

Carmellose Calcium

Calcium CMC is calcium salt of Carboxy Methyl Cellulose. It is also popularly known as Carmellose Calcium and Croscarmellose Calcium. Calcium CMC ( Carmellose Calcium ) is highly pure white powder used for tablet disintegration. Carboxymethylcellulose Calcium is insoluble in water but it swells in water and Carmellose Calcium used as super disintegrant in pharmaceutical tablet formulation. Calcium CMC helps tablets to disintegrate rapidly and also improves dissolution properties. Carmellose Calcium performs well with hard tablets where other disintegrants do not perform well

microcrystalline cellulose powder

Microcrystalline Cellulose revolutionized tableting because of its unique compressibility and carrying capacity. Its exhibits excellent properties as an excipient for solid dosages forms, compact well under minimum compression pressures, has high binding capability and creates tablets that are extremely hard & stable, yet disintegrate rapidly.

Sodium Carboxymethyl Cellulose pure /pharma/food grade

Croscarmellose Sodium is a cross linked polymer of Carboxymethyl Cellulose Sodium. Cross an insoluble, hydrophilic, highly absorbent material, rsulting in excellent swelling properties fibrous nature gives it excellent water wicking capacities. Croscarmellose Sodium provides dissolution and disintegration characteristics, thus improving bioavailability of formulation.

PHENYL 1-HYDROXY-2-NAPHTHOATE

CAS No: 132-54-7 Molecular Formula C17H12O3 1-HYDROXY-2-NAPHTHOIC ACID PHENYL ESTER 1-HYDROXY-2-NAPTHOIC ACID PHENYL ESTER AON PHENYL ESTER

Synthetic Liver Extract Liquid

SYNTHETIC LIVER EXTRACT LIQUID

5-Hydroxytryptophan (5HTP)

5-Hydroxytryptophan (5HTP) Assay -95% Uses- 5-Hydroxytryptophan (5-HTP) uses it to produce serotonin, a chemical messenger that sends signals between your nerve cells. Low serotonin levels are associated with depression, anxiety, sleep disorders, weight gain and other health problems.

Lactose Monohydrate

LACTOSE MONO HYDRATE 200 MESH

Activated Carbon

Activated carbon, also called activated charcoal, is a form of carbon processed to have small, low-volume pores that increase the surface area available for adsorption or chemical reactions.

Polymixin B Sulphate

Polymyxin B and trimethoprim ophthalmic combination is used to treat bacterial infections of the eye including conjunctivitis

Polymixin B Sulphates

Polymyxin B and trimethoprim ophthalmic combination is used to treat bacterial infections of the eye including conjunctivitis

Griseofulvin API

Griseofulvin is an antifungal medication used to treat a number of types of dermatophytoses. This includes fungal infections of the nails and scalp, as well as the skin when antifungal creams have not worked.

Atropine Sulphate

Atropine sulphate

Zinc Bacitracin

Bacitracin zinc is a medicine that is used on cuts and other skin wounds to help prevent infection. Bacitracin is an antibiotic, a medicine that kills germs. Small amounts of bacitracin zinc are dissolved in petroleum jelly to create antibiotic ointments

Neomycin Sulphate

Neomycin is an aminoglycoside antibiotic found in many topical medications such as creams, ointments, and eyedrops. Neomycin belongs to aminoglycoside class of antibiotics that contain two or more amino sugars connected by glycosidic bonds.

Calcium Pantothenate

is the calcium salt of the water-soluble vitamin B5. It is ubiquitously found in plants and animal tissues. Calcium Pantothenate or Vitamin B5 has antioxidant property. It is a growth factor in the system.

Gentamycin Sulphate

used to treat several types of bacterial infections. This may include bone infections, endocarditis, pelvic inflammatory disease, meningitis, pneumonia, urinary tract infections, and sepsis among others

PVPK 30

A polyvinyl polymer of variable molecular weight; used as suspending and dispersing agent and vehicle for pharmaceuticals; also used as blood volume expander.

Sulbactum sodium

Sulbactam Sodium is the sodium salt form of sulbactam, a beta-lactam with weak antibacterial property. Sulbactam sodium contains a beta-lactam ring and irreversibly binds to beta-lactamase at or near its active site, thereby blocking enzyme activity and preventing metabolism of other beta-lactam antibiotics.

Vitamin b6

Vitamin B-6 (pyridoxine) is important for normal brain development and for keeping the nervous system and immune system healthy.

Refined Fish Oil

Refined Fish oil has an important application in Leather Chemical Industry. Crude Fish Oil has undesirable substance present in varying amounts. These are removed by refining or processing to increase its usefulness as a starting material for the manufacture of industrial products. Refined, de-odourised, de-colourised fish oil also is an input for Pet food & Pharma Industries.

Isotretinoin Raw Material

isotretinoin api

Venetoclax

Carboprost

Carboprost

Latanoprost

Sirolimus Raw Material

sirolimus api

Melphalan

Tamsulosin

Tamsulosin

Timolol Maleate

Adapalene

Bimatoprost

Temozolomide

tolvaptan

is an aquaretic drug that functions as a selective, competitive vasopressin receptor 2 (V2) antagonist used to treat hyponatremia (low blood sodium levels) associated with congestive heart failure, cirrhosis, and the syndrome of inappropriate antidiuretic hormone (SIADH).

Tafluprost

Tafluprost:

Travaprost

Travaprost:

Carglumic Acid

Carglumic Acid

Sodium Cromoglicate

Sodium Cromoglicate

Capsaicin

DescriptionCapsaicin is an active component of chili peppers, which are plants belonging to the genus Capsicum. It is an irritant for mammals, including humans, and produces a sensation of burning in any tissue with which it comes into contact

Oxyphenonium Bromide

Oxyphenonium bromide is an antimuscarinic drug. It is used to treat gastric and duodenal ulcers and to relieve visceral spasms.

Pramoxine Hydrochloride

Pramoxine is used to temporarily relieve itching and pain caused by minor skin irritation such as minor burns/cuts/scrapes, sunburn, eczema, insect bites, cold sores, or rashes from poison ivy, poison oak, or poison sumac.

Oxybutynin Chloride or Hydrochloride

An antispasmodic used for the treatment of overactive bladder. It has a role as a muscarinic antagonist, a muscle relaxant, an antispasmodic drug, a parasympatholytic, a calcium channel blocker and a local anaesthetic. It is a tertiary amino compound and a racemate.

Diminazene aceturate

Diminazene is an anti-infective medication for animals

pramoxine

Pramocaine (also known as pramoxine or pramoxine HCI) is a topical anesthetic and antipruritic.

Embramine

Embramine is an antihistamine and anticholinergic drugs

Ipratropium Bromide

Ipratropium bromide, an anticholinergic drug, still awaits a defined role in the treatment of asthma. ... Corticosteroids, including inhaled steroids, have measurable effects on symptoms, lung function, bronchial responsiveness and inflammation associated with asthma.

Isopropamide Iodide

Isopropamide is a long-acting anticholinergic drug. It is used in the treatment of peptic ulcers and other gastrointestinal disorders involving hyperacidity and hypermotility. Chemically, it contains a quaternary ammonium group.

Glycopyrrolate

Glycopyrronium (as the bromide salt glycopyrrolate) is a synthetic anticholinergic agent with a quaternary ammonium structure. A muscarinic competitive antagonist used as an antispasmodic, in some disorders of the gastrointestinal tract, and to reduce salivation with some anesthetics

Digoxin

Digoxin is a cardiac glycoside. Digoxin inhibits the sodium potassium adenosine triphosphatase (ATPase) pump, thereby increasing intracellular calcium and enhancing cardiac contractility. This agent also acts directly on the atrioventricular node to suppress conduction, thereby slowing conduction velocity

Ritodrine

DescriptionRitodrine is a tocolytic drug used to stop premature labor

Scopine

Scopine is a tropane alkaloid found in a variety of plants including Mandragora root, Senecio mikanoides (Delairea odorata), Scopolia carniolica, and Scopolia lurida. Scopine can be prepared by the hydrolysis of scopolamine.

Sennosides

Sennosides are used to treat constipation. They may also be used to clean out the intestines before a bowel examination/surgery. Sennosides are known as stimulant laxatives. They work by keeping water in the intestines, which causes movement of the intestines.

Vinpocetine

DescriptionVinpocetine is a synthetic derivative of the vinca alkaloid vincamine. Vincamine is extracted from either the seeds of Voacanga africana or the leaves of Vinca minor

HOMATROPINE HYDROBROMIDE

This medication is used before eye examinations (e.g., refraction), before and after certain eye surgeries, and to treat certain eye conditions (e.g., uveitis). It belongs to a class of drugs known as anticholinergics. Homatropine hydrobromide works by widening (dilating) the pupil of the eye. This medication is used before eye examinations (e.g., refraction), before and after certain eye surgeries, and to treat certain eye conditions (e.g., uveitis). It belongs to a class of drugs known as anticholinergics. Homatropine hydrobromide works by widening (dilating) the pupil of the eye.

18 BETA GLYCYRRHITINIC ACID

is a pentacyclic triterpenoid derivative of the beta-amyrin type obtained from the hydrolysis of glycyrrhizic acid, which was obtained from the herb liquorice. It is used in flavoring and it masks the bitter taste of drugs like aloe and quinine. It is effective in the treatment of peptic ulcer and also has expectorant (antitussive) properties.

10-Deacetylbaccatin

10-Deacetylbaccatins are a series of closely related natural organic compounds isolated from the yew tree (Genera Taxus). 10-Deacetylbaccatin III is a precursor to the anti-cancer drug docetaxel (Taxotere)

Guaifenesin

Guaifenesin is a glyceryl guaiacolate with expectorant effects. Guaifenesin increases respiratory tract mucus secretions, acts as an irritant to gastric vagal receptors and recruits efferent parasympathetic reflexes that cause glandular exocytosis. This agent reduces the viscosity of mucus secretion by reducing adhesiveness and surface tension as well as increasing hydration of mucus. Guaifenesin promotes the efficiency of the mucociliary mechanism important in removing accumulated secretions from the upper and lower airway.

Atropine sulphate

Uses. This medication is used before eye examinations (e.g., refraction) and to treat certain eye conditions (e.g., uveitis). It belongs to a class of drugs known as anticholinergics. Atropine works by widening (dilating) the pupil of the eye.

methoxsalen

METHOXSALEAN USP

HYOSCINE HYDROBROMIDE IP

Hyoscine is isolated from the plant called Duboisia and further addition reaction gives Hyoscine hydrobromide. It is a White Crystalline Powder.

Glabridin

DescriptionGlabridin is a chemical compound that is found in the root extract of licorice. Glabridin is an isoflavane, a type of isoflavonoid. This product is part of a larger family of plant-derived molecules, the natural phenols.

Hyoscine butylbromide

Butylscopolamine is a peripherally acting antimuscarinic, anticholinergic agent. It is used to treat pain and discomfort caused by abdominal cramps, menstrual cramps, or other spasmodic activity in the digestive system. It is also effective at preventing bladder spasms. It is not a pain medication in the normal sense, since it does not directly affect pain, but rather works to prevent painful cramps and spasms from occurring.

PREGABELIN

Pregabalin is used to treat epilepsy and anxiety. It is also taken to treat nerve pain. Nerve pain can be caused by different illnesses including diabetes and shingles, or an injury.

IMATINIB MESLATE

IMATINIB MESLATE

paclitaxel

Paclitaxel is a chemotherapy drug used to treat ovarian, breast and non-small cell lung cancer. It may also be used to treat other cancers such as stomach cancer.

Colchicine

Colchicine is indicated for the prophylaxis and treatment of gout flares. It is also indicated in Familial Mediterranean fever (FMF) in children and adults of 4 years of age and older. It is important to note that this medication is not a pain reliever to be used for other painful conditions.

PHENYLEPHRINE HCL

Phenylephrine is an active ingredient that has different uses in over-the-counter (OTC) medicines. When used as a nasal decongestant, phenylephrine relieves a stuffy nose due to the common cold or other ailments. Phenylephrine also shrinks the swelling caused by hemorrhoids.

mesalazine

Mesalazine raw material

QUININE SULPHATE IP

DescriptionQuinine is a medication used to treat malaria and babesiosis. This includes the treatment of malaria due to Plasmodium falciparum that is resistant to chloroquine when artesunate is not available. While used for restless legs syndrome, it is not recommended for this purpose due to the risk of side effects

Clidinium bromide

Clidinium bromide is the bromide salt of clinidium. It is used for the symptomatic treatment of peptic ulcer disease and also to help relieve abdominal or stomach spasms or cramps due to colicky abdominal pain, diverticulitis, and irritable bowel syndrome.

AMMONIUM GLYCYRRHIZNATE B.P. (M.A.G.)

AMMONIUM GLYCYRRHIZNATE B.P. (M.A.G.)

succinic acid

succinic acid

xylitol

Xylitol is a naturally occurring five-carbon sugar alcohol found in most plant material, including many fruits and vegetables. Xylitol-rich plant materials include birch and beechwood 1. It is widely used as a sugar substitute and in "sugar-free" food products. The effects of xylitol on dental caries have been widely studied, and xylitol is added to some chewing gums and other oral care products to prevent tooth decay and dry mouth

sorbitol

Sorbitol can be used as a laxative when taken orally or as an enema. Sorbitol works as a laxative by drawing water into the large intestine, stimulating bowel movements.

xanthan gum

s a polysaccharide with many industrial uses, including as a common food additive. It is an effective thickening agent and stabilizer to prevent ingredients from separating. It can be produced from simple sugars using a fermentation process, and derives its name from the species of bacteria used,

coenzyme q10

co enzyme Q10

sucralose

sucralose raw material

silymarine

sylimarine

acesulfame potassium

Acesulfame potassium also known as acesulfame K

Folic acid

Folic acid, also known as folate or Vitamin B9, is a member of the B vitamin family and an essential cofactor for enzymes involved in DNA and RNA synthesis. More specifically, folic acid is required by the body for the synthesis of purines, pyrimidines, and methionine before incorporation into DNA or protein. Folic acid is particularly important during phases of rapid cell division, such as infancy, pregnancy, and erythropoiesis, and plays a protective factor in the development of cancer. As humans are unable to synthesize folic acid endogenously, diet and supplementation is necessary to prevent deficiencies. For example, folic acid is present in green vegetables, beans, avocado, and some fruits

Yeast Extract Powder

Widely acclaimed as an efficient and effective Yeast Extract Powder Manufacturer, supplier, trader and exporter, we are engaged in offering Yeast Extract Powder. Yeast Extract Powder Manufacturer is widely used as perfect biological culture medium. Reckoned highly for improving quality and yield rate, we are Liver Extract Powder Manufacturer providing yeast extract powder which is rich in protein, balanced essential amino acids, B complex vitamin and microelements. We are one of the prominent Yeast Extract Powder Manufacturer. Offered products are processed by our team of skilled professionals. These powders are manufactured in different compositions depending on the laboratory needs and needs of chemical industry. Customers can buy these products at reasonable figures from us, a well-known Yeast Extract Powder Manufacturer. We, Yeast Extract Powder Manufacturer hold expertise in importing, distributing and trading high quality array of Yeast Extract in the industry. This product that we are offering is water soluble ingredients that are made from yeast. The yeast extracts have an extraordinary capacity and quality to raise dough. These yeast extracts have savory taste and finely fragmented consistency that has an easy use and can mix with different ingredients. We, Yeast Extract Powder Manufacturer are offering this yeast extracts to our clients at very reasonable range of prices. We are a leading Yeast Extract Powder Manufacturer. Produced by extracting the cell contents or by removing the cell walls of yeast, yeast extract with 5% nucleotide is used as food additives or flavorings, or as nutrients for bacterial culture media. Maximum purity, precise composition with good content and high utility are the special characteristics of yeast extract. In order to keep pace with the never ending demands of customers, we, Yeast Extract Powder Manufacturer are involved into offering wide range of Yeast Extract.

Liver Extract Powder

We are a leading Liver Extract Powder Manufacturer, supplier, trader and exporter of Liver Extract Powder. Liver extract powder manufacturer is produced from specific fraction of a liver. Rich in vital nutrients including an energy producing vitamin B, Liver Extract Powder Manufacturer serves as an excellent source of proteins and vitamins. Capable of stimulating the production of red blood cells, liver extract is also used as a homeopathic medicine. A low red blood count, referred to as anemia, causes your body to feel very, very tired. We are a firm to rely on, whenever seeking high-quality Liver Extract Powder. We are emerging as the best Liver Extract Powder Manufacturer. We, Liver Extract Powder Manufacturer ensure that our clients are offered with quality-tested and finely crushed and fragmented liver extract powder. For that, we perform various quality tests on them. And moreover, the Powder provides effective results and is known for providing more than the expectations. Liver Extract is produced from specific fraction of beef liver. We, Liver Extract Powder Manufacturer provide Liver Extract powder which is rich in vital nutrients like energy provider, Vitamin B and serve as an excellent source of proteins. Liver Extract is capable of stimulating the production of red blood cells. Liver Extract powder that we, Liver Extract Powder Manufacturer offer, may also be used simply as a micro nutrition and as a homeopathic medicine as well. Liver contains many Vitamins and Minerals especially iron. Liver Extract cures hepatic dysfunction and other viral infections. Liver extract can also be used for treating certain forms of cancer. Well-known for our quality in the industry, we, Liver Extract Powder Manufacturer are engaged in offering the premium range of Liver Extract Powder. We strive to live up to our standing in the industry. Its excellent and reliable feature makes it cherished among our customers. It is high in quality and this feature goes parallel to the industry standards. We make it available in protective packaging to keep it fresh for a long time.

Sodium Ascorbate

Sodium Ascorbate

Ferrous Ascorbate

Customers can benefit from us Soya Peptone For Food Industry as we are a main manufacturer, supplier, trader and exporter of soya peptone. Soya peptone is manufactured by a controlled enzymatic hydrolysis of soy. Arranged with crude materials from vegetal cause, soya peptone is a wellspring of natural nitrogen and development components suggested very in media for particular diagnostic microbiology and modern maturation. Features: Soluble in water Consists of peptides Free amino acids mixture

Calcium Propionate

Calcium Propionate

Tryptose Acid

We are a leading manufacturer, supplier, trader and exporter of Tryptose Acid. Tryptose acid is a mixed enzymatic hydrolysate with rich nutritional value for microbiological culture media. The enzymatic hydrolysis of tryptose acid permits the preservation of vitamins and amino acids. Used in media containing blood to permit hemolytic reactions, tryptose acid is recommended in standard methods for food testing. Features: Homoegneous Broth and agar forms Vitamin preservation Specifications: Ph of 5% solution : 6.8-7.0 Nitrogen content : 12.5 to 12.8% Amino Nitrogen : 3.5 -3.7% Loss on drying : 4% Total Nitrogen: 8% Ash content : 8.0% Microbiological Limits/li> Total plate count : 5000 CFU/ gm.

Peptones

Features: Freely soluble in distilled water Aqueous solution Rich in amino acids Specifications: Ph (2% solution) 6.2 7.0 Total Nitrogen 14.2% Loss on drying 5% Amino Nitrogen 3.5% Ash 10% Sulphated Ash 9.0% Indole Test Positive Microbiological Count Total count 4500 CFU/gm

Keratin Protein Hydrolysate

keratin protein hydrolysate is a cosmetic grade keratin protein carefully monitored during its manufacture to ensure the lowest possible odor and a low ash. Keratin is a highly specialized fibrous protein, which is found in hair, feathers, wool and nails. Keratin is distinct from other proteins in that it is rich in cysteine

lactase

lactase

Yohimbine Extract

Yohimbe is an herbal supplement that is used to treat erectile dysfunction and promote weight loss. The main way that yohimbe works in the body is through blocking alpha-2 adrenergic receptors.

Sodium Propionate

Sodium Propionate

Dimethyl Glycine

Dimethyl Glycine

Brain Heart Infusion Powder

Features: Free flowing powder Dissolves in distilled water Crystal clear solution Specifications: Ph of 2% solution 7.0 -7.4 Nitrogen content 13.0% Amino Nitrogen 3.6% Loss on drying 5%Microbial limits: Total plate count 6000 CF

Soya Peptone Powder

Features: Soluble in water Consists of peptides Free amino acids mixture

Cerebro Protein Hydrolysate

Cerebro protein hydrolysate is a medication that acts at the brain level and provides us with an effective tool for improving levels of activities of daily living in patients of head injury

Casein Acid Hydrolysate

Features: Homogeneous Light precipitate High salt content Specifications: Clarity of 2% solution: Clear without suspended matter Ph of 2% solution: 6.8-7.5 Loss on drying: 3% Chlorine as (NaCl): 15 29% Total Nitrogen: 8% Amino Nitrogen 4.8% Bacterial count 1000 CFU/gm

Sodium Butyrate

Sodium Butyrate

Calcium Butyrate

Calcium Butyrate

Pitavastatin pharmaceutical raw material

CAS number 147511-69-1 Chemical Formula C25H24FNO4 "Pitavastatin is used to lower serum levels of total cholesterol, LDL-C, apolipoprotein B, and triglycerides, and raise levels of HDL-C for the treatment of dyslipidemia Pitavastatin is lipid-lowering agent that works to control the synthesis of cholesterol via competitive inhibition of the liver enzyme, 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase. As a result, a compensatory increase in LDL-receptor expression can be observed which facilitates an increase LDL catabolism."

Tretinoin pharmaceutical raw material

CAS number 302-79-4 Chemical Formula C20H28O2

Lansoprazole pharmaceutical raw material

CAS number 103577-45-3 Chemical Formula C16H14F3N3O2S "For the treatment of acid-reflux disorders (GERD), peptic ulcer disease, H. pylori eradication, and prevention of gastroinetestinal bleeds with NSAID use. Lansoprazole belongs to a class of antisecretory compounds, the substituted benzimidazoles, that do not exhibit anticholinergic or histamine H2-receptor antagonist properties, but rather suppress gastric acid secretion by specific inhibition of the (H+,K+)-ATPase enzyme system at the secretory surface of the gastric parietal cell. Because this enzyme system is regarded as the acid (proton) pump within the parietal cell, Lansoprazole has been characterized as a gastric acid-pump inhibitor, in that it blocks the final step of acid production. This effect is dose-related and leads to inhibition of both basal and stimulated gastric acid secretion irrespective of the stimulus."

Atenolol pharmaceutical raw material

CAS number 29122-68-7 Chemical Formula C14H22N2O3 "For the management of hypertention and long-term management of patients with angina pectoris Atenolol, a competitive beta(1)-selective adrenergic antagonist, has the lowest lipid solubility of this drug class. Although it is similar to metoprolol, atenolol differs from pindolol and propranolol in that it does not have intrinsic sympathomimetic properties or membrane-stabilizing activity. Atenolol is used alone or with chlorthalidone in the management of hypertension and edema."

Mebeverine raw material

CAS number 6/7/3625 Chemical Formula C25H35NO5 Mebeverineis adrugused to alleviate some of the symptoms ofirritable bowel syndrome. It works by relaxing the muscles in and around the gut

Labetalol

CAS number 36894-69-6 Chemical Formula C19H24N2O3 For the management of hypertension (alone or in combination with other classes of antihypertensive agents), as well as chronic stable angina pectoris and sympathetic overactivity syndrome associated with severe tetanus. Labetalol is used parenterally for immediate reduction in blood pressure in severe hypertension or in hypertensive crises when considered an emergency, for the control of blood pressure in patients with pheochromocytoma and pregnant women with preeclampsia, and to produce controlled hypotension during anesthesia to reduce bleeding resulting from surgical procedures.

Silodosin

CAS number 160970-54-7 Chemical Formula C25H32F3N3O4 "Treatment for symptomatic relief of benign prostatic hyperplasiaBenign prostate hyperplasia (BPH), or an enlarged prostate, is a condition found only in men and is characterized by a non-cancerous enlargement of the prostate gland. Symptoms of BPH include urinary difficulty, urinary frequency and an inability to complete bladder emptying. Silodosin is highly uroselective for the alpha (1A) receptors located in the prostate, [urethrea and bladder trigone in the lower urinary tract]. Blocking these receptors relaxes the smooth muscles, resulting in an improvement in urine flow and a reduction in BPH symptoms. The selective binding of silodosin to the alpha (1A) receptors is substantially greater than the binding to the cardiovascular-associated alpha (1B) receptors and thereby maximizes target organ activity while minimizing the potential for blood pressure effects. [Watson Pharmaceutical Inc. Press release] Silodosin is alpha 1A-adrenoceptor selective antagonist which inhibits sympathetic nerve stimulation and relaxation of smooth muscle tone in the lower urinary tract which relieves the pressure from contraction of smooth muscle. The reduction of intraurethral pressure improves voiding and storage issues associated with BPH. "

Hydrocortisone

CAS number 50-23-7 Chemical Formula C21H30O5

Mometasone Furoate

CAS number 83919-23-7 Chemical Formula C27H30Cl2O6 The inhaler is indicated for the maintenance treatment of asthma as prophylactic therapy. The nasal spray is indicated for the treatment of the nasal symptoms of seasonal allergic and perennial allergic rhinitis.

Ranitidine

Promethazine pharmaceutical raw material

CAS number 60-87-7 Chemical Formula C17H20N2S "For the treatment of allergic disorders, and nausea/vomiting. Like other H1-antagonists, promethazine competes with free histamine for binding at H1-receptor sites in the GI tract, uterus, large blood vessels, and bronchial muscle. The relief of nausea appears to be related to central anticholinergic actions and may implicate activity on the medullary chemoreceptor trigger zone."

Biotin

CAS number 58-85-5 Chemical Formula C10H16N2O3S For nutritional supplementation, also for treating dietary shortage or imbalance.Biotin is necessary for the proper functioning of enzymes that transport carboxyl units and fix carbon dioxide, and is required for various metabolic functions, including gluconeogenesis, lipogenesis, fatty acid biosynthesis, propionate metabolism, and catabolism of branched-chain amino acids.

Cis -Tosylate

Cis -Tosylate cas no- 154003-23-3

Desloratadine powder

CAS number 100643-71-8 Chemical Formula C19H19ClN2 Chemical Formula C19H19ClN2

Cilostazol pharmaceutical raw material

CAS number 73963-72-1 Chemical Formula C20H27N5O2 "For the reduction of symptoms of intermittent claudication (pain in the legs that occurs with walking and disappears with rest). Cilostazol and several of its metabolites are cyclic AMP (cAMP) phosphodiesterase III inhibitors (PDE III inhibitors), inhibiting phosphodiesterase activity and suppressing cAMP degradation with a resultant increase in cAMP in platelets and blood vessels, leading to inhibition of platelet aggregation and vasodilation."

Levocetirizine pharmaceutical raw material

CAS number 130018-77-8 Chemical Formula C21H25ClN2O3 Levocetirizine is indicated for the relief of symptoms associated with allergic rhinitis (seasonal and perennial) in adults and children 6 years of age and older.Levocetirizine, the active enantiomer of cetirizine, is an anti-histamine; its principal effects are mediated via selective inhibition of H1 receptors. The antihistaminic activity of levocetirizine has been documented in a variety of animal and human models. In vitro binding studies revealed that levocetirizine has an affinity for the human H1-receptor 2-fold higher than that of cetirizine (Ki = 3 nmol/L vs. 6 nmol/L, respectively). This increased affinity has unknown clinical relevance.

Metoclopramide pharmaceutical raw material

CAS number 364-62-5 Chemical Formula C14H22ClN3O2

Alfuzosin pharmaceutical raw material

Alfuzosin ip/bp/usp

Magaldrate powder

Magaldrate ip

Desonide

CAS number 638-94-8 Chemical Formula C24H32O6 "For the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatose. Like other topical corticosteroids, desonide has anti-inflammatory, antipruritic and vasoconstrictive properties. The drug binds to cytosolic glucocorticoid receptors. This complex migrates to the nucleus and binds to genetic elements on the DNA. This activates and represses various genes. However corticosteroids are thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor arachidonic acid. Arachidonic acid is released from membrane phospholipids by phospholipase A2."

Coenzyme Q10

Coenzyme Q10,

BECLOMETHASONE DIPROPIONATE pharmaceutical raw material

Loperamide hcl pharmaceutical raw material

CAS number 53179-11-6 Chemical Formula C29H33ClN2O2 "For the control and symptomatic relief of acute nonspecific diarrhea and of chronic diarrhea associated with inflammatory bowel disease or gastroenteritis. Also used for reducing the volume of discharge from ileostomies. In vitro and animal studies show that Loperamide acts by slowing intestinal motility and by affecting water and electrolyte movement through the bowel. Loperamide inhibits peristaltic activity by a direct effect on the circular and longitudinal muscles of the intestinal wall. It is a non-selective calcium channel blocker and binds to opioid mu-receptors. Evidence also suggests that at higher concentrations it binds to calmodulin."

Clobetasol propionate

CAS number 25122-46-7 Chemical Formula C25H32ClFO5 For short-term topical treatment of the inflammatory and pruritic manifestations of moderate to severe corticosteroid-responsive dermatoses of the scalp. The precise mechanism of the antiinflammatory activity of topical steroids in the treatment of steroid-responsive dermatoses, in general, is uncertain. However, corticosteroids are thought to act by the induction of phospholipase A2inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor arachidonic acid. Arachidonic acid is released from membrane phospholipids by phospholipase A2. Initially, however, clobetasol, like other corticosteroids, bind to the glucocorticoid receptor, which complexes, enteres the cell nucleus and modifies genetic transcription (transrepression/transactivation).

Gliclazide pharmaceutical raw material

Gliclazide ip /bp

Omeprazole pharmaceutical raw material

CAS number 73590-58-6 Chemical Formula C17H19N3O3S Omeprazole is indicated for the treatment of duodenal ulcers, benign gastric ulcers, gastroesophageal reflux disease (GERD), heartburn and other symptoms associated with GERD, erosive esophagitis, and long-term treatment of pathological hypersecretory conditions like Zollinger-Ellison syndrome, multiple endocrine adenomas, and systemic mastocytosis.

Glimepiride pharmaceutical raw material

CAS number 93479-97-1 Chemical Formula C24H34N4O5S "For concomitant use with insulin for the treatment of noninsulin-dependent (type 2) diabetes mellitus. Glimepiride, like glyburide and glipizide, is a ""second-generation"" sulfonylurea agents. Glimepiride is used with diet to lower blood glucose by increasing the secretion of insulin from pancreas and increasing the sensitivity of peripheral tissues to insulin."

Spironolactone pharmaceutical raw material

Spironolactone ip/bp

Cinacalcet pharmaceutical raw material

CAS number 226256-56-0 Chemical Formula C22H22F3N "For the treatment of secondary hyperparathyroidism in patients with Chronic Kidney Disease who are on hemodialysis or peritoneal dialysis. Also for the treatment of hypercalcemia in patients with parathyroid carcinoma. The calcium-sensing receptors on the surface of the chief cell of the parathyroid gland is the principal regulator of parathyroid hormone secretion (PTH). Cinacalcet directly lowers parathyroid hormone levels by increasing the sensitivity of the calcium sensing receptors to activation by extracellular calcium, resulting in the inhibition of PTH secretion. The reduction in PTH is associated with a concomitant decrease in serum calcium levels."

Glucosamine powder

CAS number 3416-24-8 Chemical Formula C6H13NO5 Glucosamine is usually used in the treatment of osteoarthritis, although its efficacy is still in question. Glucosamine is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids. Oral glucosamine is commonly used for the treatment of osteoarthritis. Since glucosamine is a precursor for glycosaminoglycans, and glycosaminoglycans are a major component of joint cartilage, supplemental glucosamine may help to rebuild cartilage and treat arthritis. Its use as a therapy for osteoarthritis appears safe, but there is conflicting evidence as to its effectiveness with more recent studies showing limited to no clinical benefit of use. In the United States, glucosamine is not approved by the Food and Drug Administration for medical use in humans. Since glucosamine is classified as a dietary supplement, safety and formulation are solely the responsibility of the manufacturer; evidence of safety and efficacy is not required as long as it is not advertised as a treatment for a medical condition.

Cyproheptadine

CAS number 129-03-3 Chemical Formula C21H21N For treatment of perennial and seasonal allergic rhinitis, vasomotor rhinitis, allergic conjunctivitis due to inhalant allergens and foods, mild uncomplicated allergic skin manifestations of urticaria and angioedema, amelioration of allergic reactions to blood or plasma, cold urticaria, dermatographism, and as therapy for anaphylactic reactions adjunctive to epinephrine.

Mupirocin pharmaceutical raw material

CAS number 12650-69-0 Chemical Formula C26H44O9 For the treatment ofStaphylococcinasal carriers.Mupirocin, an antibiotic produced from Pseudomonas fluorescens, is structurally unrelated to any other topical or systemic antibiotics. Mupirocin is used to treat infection caused by Staphylococcus aureus and beta-hemolytic streptococci including Streptococcus pyogenes. This antibiotic has little, if any, potential for cross-resistance with other antibiotics.

Ramipril pharmaceutical raw material

CAS number 87333-19-5 Chemical Formula C23H32N2O5 For the management of mild to severe hypertension. May be used to reduce cardiovascular mortality following myocardial infarction in hemodynamically stable individuals who develop clinical signs of congestive heart failure within a few days following myocardial infarction.[Label]To reduce the rate of death, myocardial infarction and stroke in individuals at high risk of cardiovascular events. May be used to slow the progression of renal disease in individuals with hypertension, diabetes mellitus and microalubinuria or overt nephropathy.

Isoxsuprine

CAS number 395-28-8 Chemical Formula C18H23NO3 Isoxsuprine. Isoxsuprine (used as isoxsuprine hydrochloride) is a drug used as a vasodilator in humans (under the trade name Duvadilan) and equines. Isoxsuprine is a 2adrenoreceptor agonist that causes direct relaxation of uterine andvascular smooth musclevia2receptors.

Loratadine pharmaceutical raw material

CAS number 79794-75-5 Chemical Formula C22H23ClN2O2

Amlodipine besylate

CAS number 88150-42-9 Chemical Formula C20H25ClN2O5 For the treatment of hypertension and chronic stable angina.Amlodipine decreases arterial smooth muscle contractility and subsequent vasoconstriction by inhibiting the influx of calcium ions through L-type calcium channels. Calcium ions entering the cell through these channels bind to calmodulin. Calcium-bound calmodulin then binds to and activates myosin light chain kinase (MLCK). Activated MLCK catalyzes the phosphorylation of the regulatory light chain subunit of myosin, a key step in muscle contraction. Signal amplification is achieved by calcium-induced calcium release from the sarcoplasmic reticulum through ryanodine receptors. Inhibition of the initial influx of calcium decreases the contractile activity of arterial smooth muscle cells and results in vasodilation. The vasodilatory effects of amlodipine result in an overall decrease in blood pressure. Amlodipine is a long-acting CCB that may be used to treat mild to moderate essential hypertension and exertion-related angina (chronic stable angina). Another possible mechanism is that amlodipine inhibits vascular smooth muscle carbonic anhydrase I activity causing cellular pH increases which may be involved in regulating intracelluar calcium influx through calcium channels.

Vitamin E

vitamin e

Montelukast sodium pharmaceutical raw material

CAS number 158966-92-8 Chemical Formula C35H36ClNO3S For the treatment of asthma Montelukast selectively antagonizes leukotriene D4 (LTD4) at the cysteinyl leukotriene receptor, CysLT1, in the human airway. Montelukast inhibits the actions of LTD4 at the CysLT1 receptor, preventing airway edema, smooth muscle contraction, and enhanced secretion of thick, viscous mucus.

Vitamin B1 or Thiamine

CAS number 70-16-6 Chemical Formula C12H17N4OS

Glyburide or Glibenclamide pharmaceutical raw material

CAS number 10238-21-8 Chemical Formula C23H28ClN3O5S Indicated as an adjunct to diet to lower the blood glucose in patients with NIDDM whose hyperglycemia cannot be satisfactorily controlled by diet alone.Glyburide, a second-generation sulfonylurea antidiabetic agent, lowers blood glucose acutely by stimulating the release of insulin from the pancreas, an effect dependent upon functioning beta cells in the pancreatic islets. With chronic administration in Type II diabetic patients, the blood glucose lowering effect persists despite a gradual decline in the insulin secretory response to the drug. Extrapancreatic effects may be involved in the mechanism of action of oral sulfonyl-urea hypoglycemic drugs. The combination of glibenclamide and metformin may have a synergistic effect, since both agents act to improve glucose tolerance by different but complementary mechanisms. In addition to its blood glucose lowering actions, glyburide produces a mild diuresis by enhancement of renal free water clearance. Glyburide is twice as potent as the related second-generation agent glipizide.

Ondansetron pharmaceutical raw material

CAS number 99614-02-5 Chemical Formula C18H19N3O In the adult patient population: i) orally administered ondansetron tablets and orally disintegrating tablets (ODT) are indicated for: - the prevention of nausea and vomiting associated with emetogenic cancer chemotherapy, including high dose (ie. greater than or equal to 50 mg/m2) cisplatin therapy, and radiotherapy, and - the prevention and treatment of postoperative nausea and vomiting ii) intravenously administered ondansetron injection formulations are indicated for: - the prevention of nausea and vomiting associated with emetogenic cancer chemotherapy, including high dose (ie. greater than or equal to 50 mg/m2) cisplatin therapy, and - the prevention and treatment of postoperative nausea and vomiting

Ambroxol pharmaceutical raw material

CAS number 18683-91-5 Chemical Formula C13H18Br2N2O "Ambroxol is indicated as secretolytic therapy in bronchopulmonary diseases associated with abnormal mucus secretion and impaired mucus transport. It promotes mucus clearance, facilitates expectoration and eases productive cough, allowing patients to breathe freely and deeply. Ambroxol is a mucolytic agent. Excessive Nitric oxide (NO) is associated with inflammatory and some other disturbances of airways function. NO enhances the activation of soluble guanylate cyclase and cGMP accumulation. Ambroxol has been shown to inhibit the NO-dependent activation of soluble guanylate cyclase. It is also possible that the inhibition of NO-dependent activation of soluble guanylate cyclase can suppress the excessive mucus secretion, therefore it lowers the phlegm viscosity and improves the mucociliary transport of bronchial secretions."

Cyproterone Acetate

CAS number 427-51-0 Chemical Formula C24H29ClO4 "For the palliative treatment of patients with advanced prostatic carcinoma. Cyproterone is an antiandrogen. It suppresses the actions of testosterone (and its metabolite dihydrotestosterone) on tissues. It acts by blocking androgen receptors which prevents androgens from binding to them and suppresses luteinizing hormone (which in turn reduces testosterone levels)."

Citicoline sodium powder

Citicoline(INN), also known ascytidine diphosphate-choline(CDP-Choline) or

clopidogrel bisulfate Raw material

CAS number 113665-84-2 Chemical Formula C16H16ClNO2S For the reduction of atherosclerotic events (myocardial infarction, stroke, and vascular death) in patients with atherosclerosis documented by recent stroke, recent myocardial infarction, or established peripheral arterial disease.The active metabolite of clopidogrel prevents binding of adenosine diphosphate (ADP) to its platelet receptor, impairing the ADP-mediated activation of the glycoprotein GPIIb/IIIa complex. It is proposed that the inhibition involves a defect in the mobilization from the storage sites of the platelet granules to the outer membrane. he drug specifically and irreversibly inhibits the P2Y12 subtype of ADP receptor, which is important in aggregation of platelets and cross-linking by the protein fibrin. No direct interference occurs with the GPIIb/IIIa receptor. As the glycoprotein GPIIb/IIIa complex is the major receptor for fibrinogen, its impaired activation prevents fibrinogen binding to platelets and inhibits platelet aggregation. By blocking the amplification of platelet activation by released ADP, platelet aggregation induced by agonists other than ADP is also inhibited by the active metabolite of clopidogrel.

Ursodeoxycholic acid

CAS number 128-13-2 Chemical Formula C24H40O4 "

Enalapril maleate pharmaceutical raw materials

CAS number 75847-73-3 Chemical Formula C20H28N2O5

Mizolastine pharmaceutical raw material

"CAS number 108612-45-9" Chemical Formula C24H25FN6O non-sedating antihistamine. It blocks H1receptors and is commonly fast-acting. It does not prevent the actual release of histamine from mast cells, it just prevents it binding to receptors.

Domperidone

CAS number 57808-66-9 Chemical Formula C22H24ClN5O2 "For management of dyspepsia, heartburn, epigastric pain, nausea, and vomiting.Domperidone acts as a gastrointestinal emptying (delayed) adjunct and peristaltic stimulant. The gastroprokinetic properties of domperidone are related to its peripheral dopamine receptor blocking properties. Domperidone facilitates gastric emptying and decreases small bowel transit time by increasing esophageal and gastric peristalsis and by lowering esophageal sphincter pressure. Antiemetic: The antiemetic properties of domperidone are related to its dopamine receptor blocking activity at both the chemoreceptor trigger zone and at the gastric level. It has strong affinities for the D2 and D3 dopamine receptors, which are found in the chemoreceptor trigger zone, located just outside the blood brain barrier, which - among others - regulates nausea and vomiting "

Telmisartan pharmaceutical raw material

CAS number 144701-48-4 Used alone or in combination with other classes of antihypertensives for the treatment of hypertension. Also used in the treatment of diabetic nephropathy in hypertensive patients with type 2 diabetes mellitus, as well as the treatment of congestive heart failure (only in patients who cannot tolerate ACE inhibitors).

Tamsulosin

"Used in the treatment of signs and symptoms of benign prostatic hyperplasia (reduction in urinary obstruction and relief of associated manifestations such as hesitancy, terminal dribbling of urine, interrupted or weak stream...etc.) Tamsulosin is a selective antagonist at alpha-1A and alpha-1B-adrenoceptors in the prostate, prostatic capsule, prostatic urethra, and bladder neck. At least three discrete alpha1-adrenoceptor subtypes have been identified: alpha-1A, alpha-1B and alpha-1D; their distribution differs between human organs and tissue. Approximately 70% of the alpha1-receptors in human prostate are of the alpha-1A subtype. Blockage of these receptors causes relaxation of smooth muscles in the bladder neck and prostate, and thus decreases urinary outflow resistance in men."

Lopinavir pharmaceutical raw material

CAS number 192725-17-0 Chemical Formula C37H48N4O5 Indicated in combination with other antiretroviral agents for the treatment of HIV-infection.Lopinavir inhibits the HIV viral protease enzyme. This prevents cleavage of the gag-pol polyprotein and, therefore, improper viral assembly results. This subsequently results in non-infectious, immature viral particles.

Dutasteride pharmaceutical raw material

CAS number 164656-23-9 Chemical Formula C27H30F6N2O2 "For the treatment of symptomatic benign prostatic hyperplasia (BPH) in men with an enlarged prostate gland to improve symptoms, and reduce the risk of acute urinary retention and the need for surgery. Dutasteride inhibits the conversion of testosterone to 5 alpha-dihydrotestosterone (DHT), which is the androgen primarily responsible for the initial development and subsequent enlargement of the prostate gland. Testosterone is converted to DHT by the enzyme 5 alpha-reductase, which exists as 2 isoforms, type 1 and type 2. Dutasteride is a competitive and specific inhibitor of both type 1 and type 2 5 alpha-reductase isoenzymes, with which it forms a stable enzyme complex. Dissociation from this complex has been evaluated under in vitro and in vivo conditions and is extremely slow. Dutasteride does not bind to the human androgen receptor. "

Clomifene pharmaceutical raw material

CAS number 911-45-5 Chemical Formula C26H28ClNO Used mainly in female infertility due to anovulation (e.g. due to polycystic ovary syndrome) to induce ovulation.Clomifene has both estrogenic and anti-estrogenic properties, but its precise mechanism of action has not been determined. Clomifene appears to stumulate the release of gonadotropins, follicle-stimulating hormone (FSH), and leuteinizing hormone (LH), which leads to the development and maturation of ovarian follicle, ovulation, and subsequent development and function of the coprus luteum, thus resulting in pregnancy. Gonadotropin release may result from direct stimulation of the hypothalamic-pituitary axis or from a decreased inhibitory influence of estrogens on the hypothalamic-pituitary axis by competing with the endogenous estrogens of the uterus, pituitary, or hypothalamus. Clomifene has no apparent progestational, androgenic, or antrandrogenic effects and does not appear to interfere with pituitary-adrenal or pituitary-thyroid function.

Finasteride

CAS number 98319-26-7 Chemical Formula C23H36N2O2 "For the treatment of symptomatic benign prostatic hyperplasia (BPH) in men with an enlarged prostate to: Improve symptoms, reduce the risk of acute urinary retention, reduce the risk of the need for surgery including transurethral resection of the prostate. Also used for the stimulation of regrowth of hair in men with mild to moderate androgenetic alopecia (male pattern alopecia, hereditary alopecia, common male baldness). The mechanism of action of Finasteride is based on its preferential inhibition of Type II 5a-reductase through the formation of a stable complex with the enzyme. Inhibition of Type II 5a-reductase blocks the peripheral conversion of testosterone to DHT, resulting in significant decreases in serum and tissue DHT concentrations, minimal to moderate increase in serum testosterone concentrations, and substantial increases in prostatic testosterone concetrations. As DHT appears to be the principal androgen responsible for stimulation of prostatic growth, a decrease in DHT concentrations will result in a decrease in prostatic volume (approximately 20-30% after 6-24 months of continued therapy). In men with androgenic alopecia, the mechanism of action has not been fully determined, but finasteride has shown to decrease scalp DHT concentration to the levels found in hairy scalp, reduce serum DHT, increase hair regrowth, and slow hair loss. "

dexamethasone pharmaceutical raw material

CAS number 50-02-2 Chemical Formula C22H29FO5 Injection:for the treatment of endocrine disorders, rheumatic D=disorders, collagen diseases, dermatologic diseases, allergic statesc, ophthalmic diseases, gastrointestinal diseases, respiratory diseases, hematologic disorders, neoplastic diseases, edematous states, cerebral edema. Ophthalmic ointment and solution:for the treatment of steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe. Ophthalmic solution only:for the treatment of steroid responsive inflammatory conditions of the external auditory meatus Topic cream:for relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses Oral aerosol:for the treatment of bronchial asthma and related corticosteroid responsive bronchospastic states intractable to adequate trial of conventional therapy Intranasal aerosol:for the treatment of allergic ot inflammatory nasal conditions, and nasal polyps

Halobetasol Propionate

CAS number 98651-66-2 Chemical Formula C22H27ClF2O4 For the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.Halobetasol propionate is thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor arachidonic acid. Arachidonic acid is released from membrane phospholipids by phospholipase A2. The initial interaction, however, is due to the drug binding to the cytosolic glucocorticoid receptor. After binding the receptor the newly formed receptor-ligand complex translocates itself into the cell nucleus, where it binds to many glucocorticoid response elements (GRE) in the promoter region of the target genes. The DNA bound receptor then interacts with basic transcription factors, causing the increase in expression of specific target genes.

LOSARTAN POTASSIUM

CAS number 114798-26-4 Chemical Formula C22H23ClN6O May be used as a first line agent to treat uncomplicated hypertension, isolated systolic hypertension and left ventricular hypertrophy. May be used as a first line agent to delay progression of diabetic nephropathy. Losartan may be also used as a second line agent in the treatment of congestive heart failure, systolic dysfunction, myocardial infarction and coronary artery disease in those intolerant of ACE inhibitors.

Methylprednisolone raw material

CAS number 83-43-2 Chemical Formula C22H30O5 "Adjunctive therapy for short-term administration in rheumatoid arthritis. Unbound glucocorticoids cross cell membranes and bind with high affinity to specific cytoplasmic receptors, modifying transcription and protein synthesis. By this mechanism, glucocorticoids can inhibit leukocyte infiltration at the site of inflammation, interfere with mediators of inflammatory response, and suppress humoral immune responses. The antiinflammatory actions of corticosteroids are thought to involve phospholipase A2 inhibitory proteins, lipocortins, which control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes."

Prednisolone

CAS number 50-24-8 Chemical Formula C21H28O5 For the treatment of primary or secondary adrenocortical insufficiency, such as congenital adrenal hyperplasia, thyroiditis. Also used to treat psoriatic arthritis, rheumatoid arthritis, ankylosing spondylitis, bursitis, acute gouty arthritis and epicondylitis. Also indicated for treatment of systemic lupus erythematosus, pemphigus and acute rhematic carditis. Can be used in the treatment of leukemias, lymphomas, thrombocytopenia purpura and autoimmune hemolytic anemia. Can be used to treat celiac disease, insulin resistance, ulcerative colitis and liver disorders.

Guaifenesin

CAS number 93-14-1 Chemical Formula C10H14O4 Used to assist the expectoration of phlegm from the airways in acute respiratory tract infections.Guaifenesin may act as an irritant to gastric vagal receptors, and recruit efferent parasympathetic reflexes that cause glandular exocytosis of a less viscous mucus mixture. Cough may be provoked. This combination may flush tenacious, congealed mucopurulent material from obstructed small airways and lead to a temporary improvement in dyspnea or the work of breathing.

Atorvastatin Calcium

CAS number 134523-00-5 Chemical Formula C33H35FN2O5 May be used as primary prevention in individuals with multiple risk factors for coronary heart disease (CHD) and as secondary prevention in individuals with CHD to reduce the risk of myocardial infarction (MI), stroke, angina, and revascularization procedures. May be used to reduce the risk of cardiovascular events in patients with acute coronary syndrome (ACS). May be used in the treatment of primary hypercholesterolemia and mixed dyslipidemia, homozygous familial hypercholesterolemia, primary dysbetalipoproteinemia, and/or hypertriglyeridemia as an adjunct to dietary therapy to decrease serum total and low-density lipoprotein cholesterol (LDL-C), apolipoprotein B (apoB), and triglyceride concentrations, while increasing high-density lipoprotein cholesterol (HDL-C) levels.

Telmisartan pharmaceutical raw materials

CAS number 144701-48-4 Used alone or in combination with other classes of antihypertensives for the treatment of hypertension. Also used in the treatment of diabetic nephropathy in hypertensive patients with type 2 diabetes mellitus, as well as the treatment of congestive heart failure (only in patients who cannot tolerate ACE inhibitors).

Valsartan pharmaceutical raw material

CAS number 137862-53-4 Chemical Formula C24H29N5O3 Valsartan may be used alone for the management of hypertension

Bambuterol pharmaceutical raw material

Ornidazole pharmaceutical raw material

CAS number 16773-42-5 Chemical Formula C7H10ClN3O3 Ornidazoleis an effective medicine to treat infections caused by protozoa and certain strains of anaerobic bacteria. It is used to treat infections of the stomach, intestine, urinary tract and genital area.

Mephenesin

Azathioprine

CAS number 446-86-6 Chemical Formula C9H7N7O2S

Saxagliptin pharmaceutical raw material

CAS number 361442-04-8 Chemical Formula C18H25N3O2 Treatment of type 2 diabetes mellitus to improve glycemic control in combination with other agents or as monotherapy.

Artesunate

CAS number 88495-63-0 Chemical Formula C19H28O8 "For the treatment of severe malaria caused byPlasmodium falciparumin adults and children Artesunate is an artemisinin drug capable of killing all erythrocytic stages of the malaria parasite including the ring stage, late schizonts, and the gametocytes responsible for transmission of malaria [3]. It also increases splenic clearance of infected erythrocytes by reducing cytoadherence. Artesunate and the artemisinins are the most rapid acting anti-malarial drugs. This class of drugs is ineffective against extra-erythrocytic forms, sporozoites, liver schizonts, and merozoites."

Etodolac

CAS number 41340-25-4 Chemical Formula C17H21NO3 Etodolac is a non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic and antipyretic properties. Its therapeutic effects are due to its ability to inhibit prostaglandin synthesis. It is indicated for relief of signs and symptoms of rheumatoid arthritis and osteoarthritis.For acute and long-term management of signs and symptoms of osteoarthritis and rheumatoid arthritis, as well as for the management of pain.

Dexibuprofen

CAS number 51146-56-6 Chemical Formula C13H18O2 widely used as an analgesic, anti-inflammatory and antipyretic.dexibuprofen is an active enantiomer of Ibuprofen that suppresses the prostanoid synthesis in the inflammatory cells via inhibition of the COX-2 isoform of the arachidonic acid COX.

Aceclofenac powder

Aceclofenac is a non-steroidal anti-inflammatory drug (NSAID) with marked anti-inflammatory and analgesic properties. It is reported to have a higher anti-inflammatory action or at least comparable effects than conventional NSAIDs in double-blind studie [2, 3, 5]. Aceclofenac potently inhibits the cyclo-oxygenase enzyme (COX) that is involved in the synthesis of prostaglandins, which are inflammatory mediators that cause pain, swelling, inflammation, and fever. It is orally administered for the relief of pain and inflammation in osteoarthritis, rheumatoid arthritis and ankylosing spondylitis. Aceclofenac belongs to BCS Class II as it possesses poor aqueous solubility [2]. It displays high permeability to penetrate into synovial joints where in patients with osteoarthritis and related conditions, the loss of articular cartilage in the area causes joint pain, tenderness, stiffness, crepitus, and local inflammation Aceclofenac is also reported to be effective in other painful conditions such as dental and gynaecological conditions In 1991, aceclofenac was developed as an analog of a commonly prescribed NSAID, Diclofenac, via chemical modification in effort to improve the gastrointestinal tolerability of the drug. Indicated for the relief of pain and inflammation in osteoarthritis, rheumatoid arthritis and ankylosing spondylitis.

Pepsin raw materials

Used as a pancreatic enzyme replacement in pancreatic insufficiencyIt is intended to mimic naturally produced human pepsin

Ketoconazole

CAS number 65277-42-1 Chemical Formula C26H28Cl2N4O4 For the treatment of the following systemic fungal infections: candidiasis, chronic mucocutaneous candidiasis, oral thrush, candiduria, blastomycosis, coccidioidomycosis, histoplasmosis, chromomycosis, and paracoccidioidomycosis. Ketoconazole, like clotrimazole, fluconazole, itraconazole, and miconazole, is an imidazole antifungal agent.

Pyrimethamine pharmaceutical raw material

For the treatment of toxoplasmosis and acute malaria; For the prevention of malaria in areas non-resistant to pyrimethamine Pyrimethamine is an antiparasitic compound commonly used as an adjunct in the treatment of uncomplicated, chloroquine resistant, P. falciparum malaria. Pyrimethamine is a folic acid antagonist and the rationale for its therapeutic action is based on the differential requirement between host and parasite for nucleic acid precursors involved in growth. This activity is highly selective against plasmodia and Toxoplasma gondii. Pyrimethamine possesses blood schizonticidal and some tissue schizonticidal activity against malaria parasites of humans. However, the 4-amino-quinoline compounds are more effective against the erythrocytic schizonts. It does not destroy gametocytes, but arrests sporogony in the mosquito. The action of pyrimethamine against Toxoplasma gondii is greatly enhanced when used in conjunction with sulfonamides.

Secnidazole

CAS number 3366-95-8 Chemical Formula C7H11N3O3 Indicated for the treatment of bacterial vaginosis in adult women .Secnidazole enters the bacterial cell as a prodrug without an antimicrobial activity. The drug is converted to an active form via reduction of nitro groups to radical anions by bacterial enzymes. The radical anions are thought to interfere with bacterial DNA synthesis of susceptible isolates

Betahistine

Betahistine IP

Capsaicin powder

CAS number 404-86-4 Chemical Formula C18H27NO3 The capsaicin 8% patch is indicated in the treatment of neuropathic pain associated with post-herpetic neuralgia. There are multiple topical capsaicin formulations available, including creams and solutions, indicated for temporary analgesia in muscle and join pain as well as neuropathic pain.

Serratiopeptidase plain and coated

Serratiopeptidase is a proteolytic enzyme obtained from the silkworm. It is used to reduce pain and swelling associated with conditions like back pain, arthritis, tension headaches and migraine headaches.

Vitamin b6 or Pyridoxine

CAS number 65-23-6 Chemical Formula C8H11NO3

Misoprostol

CAS number 59122-46-2 Chemical Formula C22H38O5 Indicated for the treatment of ulceration (duodenal, gastric and NSAID induced) and prophylaxis for NSAID induced ulceration. Misoprostol is also indicated for other uses that are not approved in Canada, including the medical termination of an intrauterine pregnancy used alone or in combination with methotrexate,as well as the induction of labour in a selected population of pregnant women with unfavourable cervices. This indication is avoided in women with prior uterine surgery or cesarean surgery due to an increased risk of possible uterine rupture. Misoprostol is also used for the prevention or treatment of serious postpartum hemorrhage.

Timolol

CAS number 26839-75-8 Chemical Formula C13H24N4O3S In its oral form it is used to treat high blood pressure and prevent heart attacks, and occasionally to prevent migraine headaches. In its opthalmic form it is used to treat open-angle and occasionally secondary glaucoma.

Ofloxacin powder

CAS number 82419-36-1 Chemical Formula C18H20FN3O4 For the treatment of infections (respiratory tract, kidney, skin, soft tissue, UTI), urethral and cervical gonorrhoea.Ofloxacin is a quinolone/fluoroquinolone antibiotic. Ofloxacin is bactericidal and its mode of action depends on blocking of bacterial DNA replication by binding itself to an enzyme called DNA gyrase, which allows the untwisting required to replicate one DNA double helix into two. Notably the drug has 100 times higher affinity for bacterial DNA gyrase than for mammalian. Ofloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria.

Vitamin B3 or Niacin

CAS number 59-67-6 Chemical Formula C6H5NO2 "For the treatment of type IV and V hyperlipidemia. It is indicated as ajunctive therapy. Niacin binds to Nicotinate D-ribonucleotide phyrophsopate phosphoribosyltransferase, Nicotinic acid phosphoribosyltransferase, Nicotinate N-methyltransferase and the Niacin receptor. Niacin is the precursor to nicotinamide adenine dinucleotide (NAD) and nicotinamide adenine dinucleotide phosphate (NADP), which are vital cofactors for dozens of enzymes. The mechanism by which niacin exerts its lipid lowering effects is not entirely understood, but may involve several actions, including a decrease in esterification of hepatic triglycerides. Niacin treatment also decreases the serum levels of apolipoprotein B-100 (apo B), the major protein component of the VLDL (very low-density lipoprotein) and LDL fractions."

Ciprofloxacin

Paracetamol or Acetaminophen

Chemical Formula C8H9NO2 CAS number 103-90-2 For temporary relief of fever, minor aches, and pains.

Adapalene ip/bp

CAS number 106685-40-9 Chemical Formula C28H28O3 For the topical treatment of comedo, papular and pustular acne (acne vulgaris) of the face, chest or back.

Ichthammol

Ichthammol is also referred to as ammonium bituminosulfonate or ammonium bituminosulphonate. It is an ammonium salt of dark sulfonated shale oil (bituminous schists) produced via distillation of the oil followed by sulfonation and neutralization. It is available in OTC products as an active ingredient for the treatment of skin disorders such as eczema, psoriasis and boils as it is thought to exhibit anti-inflammatory, antibacterial and antimycotic properties

Enalapril maleate pharmaceutical raw material

CAS number 75847-73-3 Chemical Formula C20H28N2O5 For the treatment of essential or renovascular hypertension and symptomatic congestive heart failure. It may be used alone or in combination with thiazide diuretics.

Calcium D Pantothenate IP or Pantothenic Acid

CAS number 79-83-4 Chemical Formula C9H17NO5 Studied for the treatment of many uses such as treatment of testicular torsion, diabetic ulceration, wound healing, acne, obesity, diabetic peripheral polyneuropathy. It has also been investigated for its hypolipidemic effects and as cholesterol lowering agent.

Levofloxacin

CAS number 100986-85-4 Chemical Formula C18H20FN3O4 For the treatment of bacterial conjunctivitis caused by susceptible strains of the following organisms:Corynebacteriumspecies,Staphylococus aureus,Staphylococcus epidermidis,Streptococcus pneumoniae,Streptococcus(Groups C/F/G), Viridans group streptococci,Acinetobacter lwoffii,Haemophilus influenzae,Serratia marcescens.

Fungal Diastase

We are manufacturing and offering Fungal Diastage for Pharma, Food and Feed grade. Pancreatic Diastase enzymes function to catalyzes the breakdown of starch into maltose. Diastase is a starch-liquefying enzyme, principally alpha-amylase, derived from porcine pancreas glands.

Thiocolchicoside

CAS number 602-41-5 Chemical Formula C27H33NO10S Thiocolchicoside is a skeletal muscle-relaxant drug used in the treatment of orthopedic, traumatic and rheumatologic disorders[18]. It is indicated as an adjuvant drug in the treatment of painful muscle contractures and is indicated in acute spinal pathology, for adults and adolescents 16 years of age and older[15]. Recent studies have examined its effect on muscle tone, stiffness, contractures, and soreness experienced by athletes during sporting competitions[20

Deflazacort raw material

CAS number 14484-47-0 Chemical Formula C25H31NO6 "is a corticosteroid indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients 5 years of age and older Deflazacort is a corticosteroid prodrug, whose active metabolite, 21-desDFZ, acts through the glucocorticoid receptor to exert anti-inflammatory and immunosuppressive effects. The precise mechanism by which deflazacort exerts its therapeutic effects in patients with DMD is unknown."

Betamethasone Dipropionate pharmaceutical raw material

CAS number 378-44-9 Chemical Formula C22H29FO5 Topical use (cream, lotion and ointment): for relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. Topical use (foam): relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses of the scalp. Systemic use: for the treatment of edocrine disorders, rheumatic disorders, collagen diseases, dermatological diseases, allergic states, ophthalmic diseases, respiratory diseases, hematologic disorders, neoplastic diseases, edematous states, gastrointestinal diseases, tuberculous meningitis and trichinosis.

Prasugrel hcl

CAS number 150322-43-3 Chemical Formula C20H20FNO3S Indicated in combination with acetylsalicylic acid (ASA) to prevent atherothrombotic events in patients with acute coronary syndrome (ACS) who are to be managed with percutaneous coronary intervention (PCI). May be used in patients with unstable angina (UA), non-ST elevation myocardial infarction (NSTEMI), ST-elevation myocardial infarction (STEMI) who are to be managed with PCI. Prasugrel is not recommended in patients 75 years of age or greater, those that weigh<60kg, and patients with a history of stroke or transient ischemic attack due to increased risk of fatal and intracranial bleeding.

Terbinafine pharmaceutical raw material

CAS number 91161-71-6 Chemical Formula C21H25N

Pantoprazole sodium

CAS number 102625-70-7 Chemical Formula C16H15F2N3O4S " Pantoprazole Injection: Treatment of gastroesophageal reflux disease associated with a history of erosive esophagitis Pantoprazole for injection is indicated for short-term treatment (7-10 days) of patients having gastroesophageal reflux disease (GERD) with a history of erosive esophagitis, as an alternative to oral medication in patients who are unable to continue taking pantoprazole delayed-release tablets. Safety and efficacy of pantoprazole injection as the initial treatment of patients having GERD with a history of erosive esophagitis have not been demonstrated at this time [Label]. Pathological Hypersecretion Associated with Zollinger-Ellison Syndrome Pantoprazole for injection is indicated for the treatment of pathological hypersecretory conditions associated with Zollinger-Ellison Syndrome or other neoplastic conditions "

Ibuprofen pharmaceutical raw material

CAS number 15687-27-1 Chemical Formula C13H18O2 Ibuprofen is the most commonly used and prescribed NSAID. It is very common over the counter medication widely used as an analgesic, anti-inflammatory and antipyretic.

Voglibose

CAS number 83480-29-9 Chemical Formula C10H21NO7 For the treatment of diabetes. It is specifically used for lowering post-prandial blood glucose levels thereby reducing the risk of macrovascular complications. Voglibose, an alpha-glucosidase inhibitor, is a synthetic compound with potent and enduring therapeutic efficacies against disorders of sensory, motor and autonomic nerve systems due to diabetes mellitus. The drug was approved in Japan in 1994 for the treatment of diabetes, and it is under further investigation by Takeda for the treatment of impaired glucose tolerance. Alpha-glucosidase inhibitors are oral anti-diabetic drugs used for diabetes mellitus type 2 that work by preventing the digestion of complex carbohydrates (such as starch). Complex carbohydrates are normally converted into simple sugars (monosaccharides) which can be absorbed through the intestine. Hence, alpha-glucosidase inhibitors reduce the impact of complex carbohydrates on blood sugar.

Indometacin

Chemical Formula C19H16ClNO4 For moderate to severe rheumatoid arthritis including acute flares of chronic disease, ankylosing spondylitis, osteoarthritis, acute painful shoulder (bursitis and/or tendinitis) and acute gouty arthritis.Indomethacin, a NSAIA, with analgesic and antipyretic properties exerts its pharmacological effects by inhibiting the synthesis of prostaglandins involved in pain, fever, and inflammation. Indomethacin inhibits the catalytic activity of the COX enzymes, the enzymes responsible for catalyzing the rate-limiting step in prostaglandin synthesis via the arachidonic acid pathway. Indomethacin is known to inhibit two well-characterized isoforms of COX, COX-1 and COX-2, with greater selectivity for COX-1. COX-1 is a constitutively expressed enzyme that is involved in gastric mucosal protection, platelet and kidney function. It catalyzes the conversion of arachidonic acid to prostaglandin (PG) G2 and PGG2 to PGH2. COX-1 is involved in the synthesis pathways of PGE2, PGD2, PDF2a, PGI2 (also known as prostacyclin) and thromboxane A2 (TXA2). COX-2 is constitutively expressed and highly inducible by inflammatory stimuli. It is found in the central nervous system, kidneys, uterus and other organs. It also catalyzes the conversion of arachidonic acid to PGG2 and PGG2 to PGH2. In the COX-2-mediated pathway, PGH2 is subsequently converted to PGE2 and PGI2 (also known as prostacyclin). PGE2 is involved in mediating inflammation, pain and fever. Decreasing levels of PGE2 leads to decreased inflammation.

Bisacodyl ip/bp

CAS number 603-50-9 Chemical Formula C22H19NO4 Indicated for cleansing of the colon as a preparation for colonoscopy in adults.

Itraconazole

CAS number 84625-61-6 Chemical Formula C35H38Cl2N8O4 "For the treatment of the following fungal infections in immunocompromised and non-immunocompromised patients: pulmonary and extrapulmonary blastomycosis, histoplasmosis, aspergillosis, and onychomycosis Itraconazole is an imidazole/triazole type antifungal agent. Itraconazole is a highly selective inhibitor of fungal cytochrome P-450 sterol C-14 -demethylation via the inhibition of the enzyme cytochrome P450 14-demethylase. This enzyme converts lanosterol to ergosterol, and is required in fungal cell wall synthesis. The subsequent loss of normal sterols correlates with the accumulation of 14 -methyl sterols in fungi and may be partly responsible for the fungistatic activity of fluconazole. Mammalian cell demethylation is much less sensitive to fluconazole inhibition. Itraconazole exhibits in vitro activity against Cryptococcus neoformans and Candida spp. Fungistatic activity has also been demonstrated in normal and immunocompromised animal models for systemic and intracranial fungal infections due to Cryptococcus neoformans and for systemic infections due to Candida albicans."

Glipizide pharmaceutical raw material

CAS number 29094-61-9 Chemical Formula C21H27N5O4S "For use as an adjunct to diet for the control of hyperglycemia and its associated symptomatology in patients with non-insulin-dependent diabetes mellitus (NIDDM; type II), formerly known as maturity-onset diabetes, after an adequate trial of dietary therapy has proved unsatisfactory. Glipizide, a second-generation sulfonylurea, is used with diet to lower blood glucose in patients with diabetes mellitus type II. The primary mode of action of glipizide in experimental animals appears to be the stimulation of insulin secretion from the beta cells of pancreatic islet tissue and is thus dependent on functioning beta cells in the pancreatic islets. In humans glipizide appears to lower the blood glucose acutely by stimulating the release of insulin from the pancreas, an effect dependent upon functioning beta cells in the pancreatic islets. In man, stimulation of insulin secretion by glipizide in response to a meal is undoubtedly of major importance. Fasting insulin levels are not elevated even on long-term glipizide administration, but the postprandial insulin response continues to be enhanced after at least 6 months of treatment. Some patients fail to respond initially, or gradually lose their responsiveness to sulfonylurea drugs, including glipizide."

Methyl nicotinate pharmaceutical raw material

CAS number 93-60-7 Chemical Formula C7H7NO2 Indicated for the temporary relief of aches and pains in muscles, tendons, and joints. Following topical administration, methyl nicotinate acts as a peripheral vasodilator to enhance local blood flow at the site of application. It induced vasodilation of the peripheral blood capillaries which are located in the dermal papillae of upper dermis layers adjacent to the epidermisdermis junction During tissue penetration at the dermis, methyl nicotinate is hydrolyzed to nicotinic acid In human volunteers, topical administration of methyl nicotinate caused vasodilation-induced generalized cutaneous erythema

Prulifloxacin pharmaceutical raw material

CAS number 123447-62-1 Chemical Formula C21H20FN3O6S Prulifloxacin has been investigated for the treatment of Urinary Tract Infection.

Meloxicam pharmaceutical raw material

CAS number 71125-38-7 Chemical Formula C14H13N3O4S2 For symptomatic treatment of arthritis and osteoarthritis.Meloxicam is an nonsteroidal anti-inflammatory drug (NSAID) with analgesic and antipyretic properties. Prostaglandins are substances that contribute to inflammation of joints. Meloxicam inhibits prostaglandin synthetase (cylooxygenase 1 and 2) and leads to a decrease of the synthesis of prostaglandins, therefore, inflammation is reduced.

Naproxen sodium pharmaceutical raw material

Naproxen sodium ip/bp CAS number 22204-53-1 Chemical Formula C14H14O3 For the treatment of rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, tendinitis, bursitis, and acute gout. Also for the relief of mild to moderate pain and the treatment of primary dysmenorrhea. Naproxen is a member of the arylacetic acid group of nonsteroidal anti-inflammatory drugs (NSAIDs). Naproxen has analgesic and antipyretic properties. As with other NSAIDs, its mode of action is not fully understood; however, its ability to inhibit prostaglandin synthesis may be involved in the anti-inflammatory effect.

Fluconazole

CAS number 86386-73-4 Chemical Formula C13H12F2N6O Fluconazole is a very selective inhibitor of fungal cytochrome P450 dependent enzymelanosterol 14--demethylase. This enzyme works to convertlanosteroltoergosterol, which is necessary for fungal cell wall synthesis. Specifically, the free nitrogen atom of the azole ring of fluconazole binds an iron atom within the heme group of the enzyme. This prevents the activation of oxygen and, as a result, the demethylation of lanosterol, which stops the process of ergosterol biosynthesis. Methylated sterols accumulate in the fungal cellular membrane, resulting in an arrest of fungal cell growth

Diacerein

"Diacerein is a prodrug which is metabolized to rhein. It is currently approved in France for the treatment of osteoarthritis although the use of diacerein is restricted due to the side effects including sevre diarrhea[6]. Diacerein is under investigation for the treatment of Insulin Resistance, Diabetes Mellitus (Type 2), and Diabetes-Related Complications. For the treatment of osteoarthritis affecting the hip or knee" Chemical Formula C19H12O8 CAS number 13739-02-1

Doxycycline pharmaceutical raw material

Drotaverine hcl

CAS number 14009-24-6 Chemical Formula C24H31NO4 Used in the treatment of functional bowel disorders and alleviating pain in renal colic. rotaverine inhibits phosphodiesterases hydrolysing cAMP, thereby increasing cAMP concentration, decreasing Ca uptake of the cells and changing the distribution of calcium among the cells. It may also have minor allosteric calcium channel blocking properties.

Mebendazole pharmaceutical raw material

Mebendazole ip/bp/usp CAS number 31431-39-7 Chemical Formula C16H13N3O3 For the treatment ofEnterobius vermicularis(pinworm),Trichuris trichiura(whipworm),Ascaris lumbricoides(common roundworm),Ancylostoma duodenale(common hookworm),Necator americanus(American hookworm) in single or mixed infections. Mebendazole causes degenerative alterations in the tegument and intestinal cells of the worm by binding to the colchicine-sensitive site of tubulin, thus inhibiting its polymerization or assembly into microtubules. The loss of the cytoplasmic microtubules leads to impaired uptake of glucose by the larval and adult stages of the susceptible parasites, and depletes their glycogen stores. Degenerative changes in the endoplasmic reticulum, the mitochondria of the germinal layer, and the subsequent release of lysosomes result in decreased production of adenosine triphosphate (ATP), which is the energy required for the survival of the helminth. Due to diminished energy production, the parasite is immobilized and eventually dies.

Anastrozole

CAS number 120511-73-1 Chemical Formula C17H19N5 Anastrozole is a drug indicated in the treatment of breast cancer in post-menopausal women. It is used both in adjuvant therapy (i.e. following surgery) and in metastatic breast cancer. It decreases the amount of estrogens that the body makes. Anastrozole belongs in the class of drugs known as aromatase inhibitors. It inhibits the enzyme aromatase, which is responsible for converting androgens (produced by women in the adrenal glands) to estrogens. For adjuvant treatment of hormone receptor positive breast cancer , as well as hormonal treatment of advanced breast cancer in post-menopausal women. Has also been used to treat pubertal gynecomastia and McCune-Albright syndrome; however, manufacturer states that efficacy for these indications have not been established.

Cabergoline pharmaceutical raw material

CAS number 81409-90-7 Chemical Formula C26H37N5O2 For the treatment of hyperprolactinemic disorders, either idiopathic or due to prolactinoma (prolactin-secreting adenomas). May also be used to manage symptoms of Parkinsonian Syndrome as monotherapy during initial symptomatic management or as an adjunct to levodopa therapy during advanced stages of disease.

Ascorbic acid IP

CAS number 50-81-7 Chemical Formula C6H8O6 Used to treat vitamin C deficiency, scurvy, delayed wound and bone healing, urine acidification, and in general as an antioxidant. It has also been suggested to be an effective antiviral agent.

Folic Acid ip/bp/usp

CAS number 59-30-3 Chemical Formula C19H19N7O6 For treatment of folic acid deficiency, megaloblastic anemia and in anemias of nutritional supplements, pregnancy, infancy, or childhood.

Cetirizine pharmaceutical raw material

CAS number 83881-51-0 Chemical Formula C21H25ClN2O3 For the relief of symptoms associated with seasonal allergic rhinitis, perennial allergic rhinitis and the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria

Mefenamic Acid

CAS number 61-68-7 Chemical Formula C15H15NO2 For the treatment of rheumatoid arthritis, osteoarthritis, dysmenorrhea, and mild to moderate pain, inflammation, and fever.

Phenylephrine

Phenylephrine is mainly used to treat nasal congestion, but may also be useful in treating hypotension and shock, hypotension during spinal anaesthesia, prolongation of spinal anaesthesia, paroxysmal supraventricular tachycardia, symptomatic relief of external or internal hemorrhoids, and to increase blood pressure as an aid in the diagnosis of heart murmurs. Phenylephrine is a powerful vasoconstrictor. It is used as a nasal decongestant and cardiotonic agent. Phenylephrine is a postsynaptic 1-receptor agonist with little effect on -receptors of the heart. Parenteral administration of phenylephrine causes a rise in systolic and diastolic pressures, a slight decrease in cardiac output, and a considerable increase in peripheral resistance; most vascular beds are constricted, and renal, splanchnic, cutaneous, and limb blood flows are reduced while coronary blood flow is increased. Phenelephrine also causes pulmonary vessel constriction and subsequent increase in pulmonary arterial pressure. Vasoconstriction in the mucosa of the respiratory tract leads to decreased edema and increased drainage of sinus cavities.

Cetrimide pharmaceutical raw material

Cetrimide is an antiseptic which is a mixture of differentquaternary ammonium saltsincludingcetrimonium bromide(CTAB).

Warfarin Sodium

CAS number 81-81-2 Chemical Formula C19H16O4 For the treatment of retinal vascular occlusion, pulmonary embolism, cardiomyopathy, atrial fibrillation and flutter, cerebral embolism, transient cerebral ischaemia, arterial embolism and thrombosis.

Tranexamic acid

CAS number 1197-18-8 Chemical Formula C8H15NO2 For use in patients with hemophilia for short term use (two to eight days) to reduce or prevent hemorrhage and reduce the need for replacement therapy during and following tooth extraction. It can also be used for excessive bleeding in menstruation, surgery, or trauma cases. Tranexamic acid is an antifibrinolytic that competitively inhibits the activation of plasminogen to plasmin. Tranexamic acid is a competitive inhibitor of plasminogen activation, and at much higher concentrations, a noncompetitive inhibitor of plasmin, i.e., actions similar to aminocaproic acid. Tranexamic acid is about 10 times more potent in vitro than aminocaproic acid. Tranexamic acid binds more strongly than aminocaproic acid to both the strong and weak receptor sites of the plasminogen molecule in a ratio corresponding to the difference in potency between the compounds. Tranexamic acid in a concentration of 1 mg per mL does not aggregate platelets in vitro. In patients with hereditary angioedema, inhibition of the formation and activity of plasmin by tranexamic acid may prevent attacks of angioedema by decreasing plasmin-induced activation of the first complement protein (C1).

Clotrimazole

CAS number 23593-75-1 Chemical Formula C22H17ClN2 "Clotrimazole topical cream is indicated for the topical treatment of the following dermal infections Tinea pedis, tinea cruris, and tinea corporis due to Trichophyton rubrum, Trichophyton mentagrophytes, Epidermophyton floccosum Candidiasis due to Candida albicans Tinea versicolor due to Malassezia furfur Diaper rash infected by Candida albicans"

Cyanocobalamin raw material

CAS number 68-19-9 Chemical Formula C63H88CoN14O14P For treatment of pernicious anemia (due to lack of or inhibition of intrinsic factor) and for prevention and treatment of vitamin B 12 deficiency

Azithromycin pharmaceutical raw material

Azithromycin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria in order to prevent the development antimicrobial resistance and maintain the efficacy of azithromycin Azithromycin is indicated for the treatment of patients with mild to moderate infections caused by susceptible strains of the microorganisms listed in the specific conditions below. Recommended dosages, duration of therapy and considerations for various patient populations may vary among these infections. Refer to the FDA label and "Indications" section of this drug entry for detailed information

Hydroxyprogesterone caproate

CAS number 630-56-8 Chemical Formula C27H40O4 Hydroxyprogesterone caproate is indicated for the prevention of spontaneous preterm births in singleton pregnancies in women who have previously had a spontaneous preterm birth.

Etamsylate

It is believed to work by increasingcapillaryendothelialresistance and promotingplateletadhesion. It also inhibitsbiosynthesisand action of thoseprostaglandinswhich cause platelet disaggregation,vasodilationand increased capillary permeability.

Mefenamic acid raw material

CAS number 61-68-7 Chemical Formula C15H15NO2 "Mefenamic acid, an anthranilic acid derivative, is a member of the fenamate group of nonsteroidal anti-inflammatory drugs (NSAIDs). It exhibits anti-inflammatory, analgesic, and antipyretic activities. Similar to other NSAIDs, mefenamic acid inhibits prostaglandin synthetase. For the treatment of rheumatoid arthritis, osteoarthritis, dysmenorrhea, and mild to moderate pain, inflammation, and fever."

Tinidazole pharmaceutical raw material

CAS number 19387-91-8 Chemical Formula C8H13N3O4S "For the treatment of trichomoniasis caused byT. vaginalisin both female and male patients. Also for the treatment of giardiasis caused byG. duodenalisin both adults and pediatric patients older than three years of age and for the treatment of intestinal amebiasis and amebic liver abscess caused byE. histolyticain both adults and pediatric patients older than three years of age. Tinidazole is a synthetic antiprotozoal agent. Tinidazole demonstrates activity both in vitro and in clinical infections against the following protozoa: Trichomonas vaginalis, Giardia duodenalis (also termed G. lamblia), and Entamoeba histolytica. Tinidazole does not appear to have activity against most strains of vaginal lactobacilli."

Nimesulide pharmaceutical raw material

CAS number 51803-78-2 Chemical Formula C13H12N2O5S For the treatment of acute pain, the symptomatic treatment of osteoarthritis and primary dysmenorrhoea in adolescents and adults above 12 years old.

Chlorphenamine Maleate ip/bp

Mefloquine pharmaceutical raw material

CAS number 53230-10-7 Chemical Formula C17H16F6N2O For the treatment of mild to moderate acute malaria caused by Mefloquineuine-susceptible strains ofPlasmodium falciparum(both chloroquine-susceptible and resistant strains) or byPlasmodium vivax. Also for the prophylaxis ofPlasmodium falciparumandPlasmodium vivaxmalaria infections, including prophylaxis of chloroquine-resistant strains ofPlasmodium falciparum. Mefloquine is an antimalarial agent which acts as a blood schizonticide. Mefloquine is active against the erythrocytic stages of Plasmodium species. However, the drug has no effect against the exoerythrocytic (hepatic) stages of the parasite. Mefloquine is effective against malaria parasites resistant to chloroquine. Mefloquine is a chiral molecule. According to some research, the (+) enantiomer is more effective in treating malaria, and the (-) enantiomer specifically binds to adenosine receptors in the central nervous system, which may explain some of its psychotropic effects.

Ethyl Oleate ip

Ethyl oleateis a long-chain fatty acidethylester resulting from the formal condensation of the carboxy group of oleic acid with the hydroxy group of ethanol. It has a role as a plant metabolite and an acaricide. It derives from an oleic acid.

Metronidazole raw material

Chemical Formula C6H9N3O3

Methylcobalamin

CAS number 13422-55-4 Chemical Formula C63H91CoN13O14P Methylcobalamin is also used in the treatment ofperipheral neuropathy,diabetic neuropathy, and as a preliminary treatment foramyotrophic lateral sclerosis

Cefuroxime Axetil

CAS number 55268-75-2 Chemical Formula C16H16N4O8S For the treatment of many different types of bacterial infections such as bronchitis, sinusitis, tonsillitis, ear infections, skin infections, gonorrhea, and urinary tract infections.

Metformin pharmaceutical raw material

CAS number 657-24-9 Chemical Formula C4H11N5 For use as an adjunct to diet and exercise in adult patients (18 years and older) with non-insulin dependent diabetes mellitus. Metformin may also be used for the management of metabolic and reproductive abnormalities associated with polycystic ovary syndrome (PCOS). Metformin may be used concomitantly with a sulfonylurea or insulin to improve glycemic control in adults Metformin decreases hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization. Unlike sulfonylureas, metformin does not produce hypoglycemia in either patients with type 2 diabetes or normal subjects (except in special circumstances) and does not cause hyperinsulinemia. With metformin therapy, insulin secretion remains unchanged while fasting insulin levels and day-long plasma insulin response may actually decrease

Trimethoprim pharmaceutical raw material

CAS number 738-70-5 Chemical Formula C14H18N4O3

Albendazole pharmaceutical raw material

"CAS number 54965-21-8" Chemical Formula C12H15N3O2S For the treatment of parenchymal neurocysticercosis due to active lesions caused by larval forms of the pork tapeworm,Taenia soliumand for the treatment of cystic hydatid disease of the liver, lung, and peritoneum, caused by the larval form of the dog tapeworm,Echinococcus granulosus.

Tazobactam SODIUM pharmaceutical raw material

CAS number 89786-04-9 Chemical Formula C10H12N4O5S Used in combination with piperacillin to broaden the spectrum of piperacillin antibacterial action.Tazobactam is a compound which inhibits the action of bacterial beta-lactamases. It is added to the extended spectrum beta-lactam antibiotic piperacillin.

Ketorolac

CAS number 74103-06-3 Chemical Formula C15H13NO3 "For the short-term (~5 days) management of moderately severe acute pain that requires analgesia at the opioid level, usually in a postoperative setting. Ketorolac, an antiinflammatory agent with analgesic and antipyretic properties, is used to treat osteoarthritis and control acute pain. It is a peripherally acting analgesic. The biological activity of ketorolac tromethamine is associated with the S-form. Ketorolac tromethamine possesses no sedative or anxiolytic properties."

Diclofenac sodium/potassium pharmaceutical raw material

is a nonsteroidal anti-inflammatory drug used to treat pain and inflammatory diseases such as gout. It is taken by mouth or applied to the skin. Improvements in pain typically occur within half an hour and last for as much as eight hours.