Bulk drugs- API-Pharmaceutical Raw material.

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.

Coenzyme Q10,

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.

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.

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.

Diminazene is an anti-infective medication for animals

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.

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

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.

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

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.

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."

Embramine is an antihistamine and anticholinergic drugs

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.

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.

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.

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.

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 "

"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.

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.

METHOXSALEAN USP

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. "

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.

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."

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)

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.

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.

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.

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

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."

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.

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.

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.

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.

CAS number 738-70-5 Chemical Formula C14H18N4O3

Chemical Formula C6H9N3O3

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

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."

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.

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."

Dextrose Monohydrate

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

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.

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.

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

SYNTHETIC LIVER EXTRACT LIQUID