Our Products
Our offered Product range includes Glimepiride, Nifedipine, Rosuvastatin Calcium, Fluconazole Powder and Atorvastatin Calcium.
Treating Type 2 Diabetes in Patients Who Cannot Control Blood Sugar Levels By Diet and Exercise Alone. It May Be Used Alone or in Combination with other Antidiabetic Medicines. Glimepiride is a Sulfonylurea Antidiabetic Medicine. It Works By Causing the Pancreas to Release Insulin, Which Helps to Lower Blood Sugar.it is Sometimes Classified as Either the First Third Generation Sulfonylurea , or as Second-generation. Controlling High blood Sugar helps Prevent kidney damage, Blindness, Nerve Problems, Loss of Limbs and Sexual Function Problems. Proper Control of Diabetes may also Lessen Your Risk of A heart Attack or Stroke. Glimepiride Belongs to Class of Drugs Known as Sulfonylureas. It Lowers Blood Sugar By Causing the Release of Your Body's Natural Insulin. Glimepiride is Very Potent and Has a Longer Duration of Action.
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Nifedipine Is A Dihydropyridine Calcium Channel Blockerthat Primarily Blocks L-type Calcium Channels. Its Main Uses Are As An Antianginal (Especially In Prinzmetal's Angina) And Antihypertensive, Although A Large Number Of Other Indications Have Recently Been Found For This Agent, Such As Raynaud's Phenomenon, Premature Labor, And Painful Spasms Of The Esophagus Such As In Cancer And Tetanus Patients. It Is Also Commonly Used For The Small Subset Of Pulmonary Hypertension Patients Symptoms Respond To Calcium Channel Blockers. Nifedipine Is Used To Treat Hypertension (High Blood Pressure) & Angina (Chest Pain). It Works By Relaxing The Muscles Of Your Heart And Blood Vessels. It Is Also Used For The Management Of Vasospastic Angina, Chronic Stable Angina, Hypertension May Be Used As A First Line Agent For Left Ventricular Hypertrophy And Isolated Systolic Hypertension (Long-acting Agents).
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Rosuvastatin Calcium Is The Calcium Salt Form Of Rosuvastatin, A Statin With Antilipidemic Activity. Rosuvastatin Selectively And Competitively Binds To And Inhibits Hepatic Hydroxymethyl-glutaryl Coenzyme A (Hmg-coa) Reductase, The Enzyme Which Catalyzes The Conversion Of Hmg-coa To Mevalonate, A Precursor Of Cholesterol. This Leads To A Decrease In Hepatic Cholesterol Levels And Increase In Uptake Of Ldl Cholesterol. It Is Synthetic Lipid Lowering Agent & In Addition To Anti-atherosclerotic Benefit, It Also Exhibits Anti-inflammatory, Cardioprotective And Anti-platelet Activities. Separately, Rosuvastatin Down Regulates Erk, P38mapk, Matrix Metalloproteinases 2 And 9 (Mmp2/9), And Pai Expression, Inhibiting Migration And Proliferation Of Vascular Smooth Muscle Cells. Additionally, Rosuvastatin Inhibits Activation Of Nadph Oxidase And Pkc, Decreasing Platelet Recruitment And Activation In Vitro And Ex Vivo.
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Fluconazole Used for Treating and Preventing Certain Yeast and Fungal Infections. Fluconazole is An Azole Antifungal and Kills Sensitive Fungi By Interfering with the Formation of the Fungal Cell Membrane fluconazole is An Antifungal Medication that is Administered Orally or Intravenously. It is Used to Treat a Variety of Fungal Infections, Especially candida infections of the Vagina ("yeast Infections'), Mouth, Throat, and Bloodstream. It is also Used to Prevent Infections in People with Weak Immune Systems, Including Those with Neutropenia Due to Cancer Chemotherapy, Transplant Patients, Those with Advanced Hiv Infections, and Premature Babies. Its Mechanism of Action Involves Interfering with Synthesis of the Fungal Cell Membrane. Fluconazole, the First of a New Subclass of Synthetic Triazole Antifungal agents, is Available as Tablets for Oral Administration, as a Powder for Oral Suspension, and as a Sterile Solution for Intravenous Use in Glass and Plastic Containers.
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Atorvastatin is in a Group of Drugs Called Hmg Coa Reductase Inhibitors, or "statins." Atorvastatin Reduces Levels of "bad" Cholesterol (low-den Sity Lipoprotein, or Ldl) and Triglycerides in the Blood, While Increasing Levels of "good" Cholesterol (high-density Lipoprotein, or HDL). Atorvastatin is Used to Treat high Cholesterol, and to Lower the Risk of Stroke, Heart Attack, or other Heart Complications in People with Type 2 Diabetes, Coronary Heart Disease, or other Risk Factors. Atorvastatin is Used in Adults and Children Who are At Least 10 Years Old. Atorvastatin May also Be Used for Purposes Not Listed in this Medication Guide.
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Fluticasone Propionate belongs to a Class of Drugs Known as Corticosteroids, Specifically glucocorticoids, Which Are hormones that Predominantly Affect the Metobolism of Carbohydrates and to a Lesser Extent, fat and protein. It is Used to Treat asthma, allergic Rhinitis, nasal Polyps, Various skin Disorders and Crohn's Disease and Ulcerative Colitis. It is also Used to Treat eosinophilic Esophagitis. Fluticasone is a Synthetic Corticosteroid. the Exact Mechanism of Action of Fluticasone is Not Known; However, It Stimulates Glucocorticoid Receptors in Humans that Produces a Potent Anti-inflammatory Response. Fluticasone Propionate, a Corticosteroid having the Chemical Name S-(fluoromethyl) 6α, 9-difluoro-11β, 17-dihydroxy-16α-methyl-3oxoandrosta-1, 4-diene-17β-carbothioate, 17-propionate & Following Chemical Structure
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Topiramate is a sulfamate-substituted monosaccharide with anti- convulsant property. Although the mechanism of action has not been fully elucidated, topiramate antagonizeskainateampa subtype of the glutamate receptors, which are ligand-activated cation channels that mediate the fast component of excitatory postsynaptic currents in neurons of the central nervous system. This antagonistic action results in stabilizing hyper-excited neural membranes, inhibiting repetitive neuronal firing & decreasing propagation of synaptic impulses, thereby impedes seizure occurrences. In addition, this agent augments gamma-aminobenzoic acid (gaba) activity & thereby attenuating gabanergic inhibitory transmission.
Linagliptin Is Active Ingredient, An Orally Active Inhibitor Of The Dipeptidyl Peptidase-4 (Dpp-4) Enzyme. Treating Type 2 Diabetes In Patients Who Cannot Control Blood Sugar Levels By Diet And Exercise Alone. It Is Used Along With Diet And Exercise. It May Be Used Alone Or With Other Antidiabetic Medicines. It Works By Increasing The Amount Of Insulin Released By Your Body And Decreasing The Amount Of Sugar Made By Your Body. Linagliptin Is A Potent, Orally Bioavailable Dihydropurinedione-based Inhibitor Of Dipeptidyl Peptidase 4 (Dpp-4), With Hypoglycemic Activity. The Inhibition Of Dpp-4 By Linagliptinappears To Be Longer Lasting Than That By Some Other Dpp-4 Inhibitors Tested.
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Benzocaine is A local Anesthetic commonly Used as A topical pain Reliever or in Cough Drops. It is the Active Ingredient in Many Over-the-counter anesthetic ointments such as Products For oral Ulcers. It is also Combined With antipyrine to Form a/b Otic Drops to Relieve Ear Pain and Remove earwax. Benzocaine is The ethyl ester of p-aminobenzoic Acid (paba). It Can Be Prepared from Paba And ethanol by fischer Esterificationor Via the Reduction of Ethyl p-nitrobenzoate. Benzocaine is Sparingly Soluble in Water; It is More Soluble in Dilute Acids and Very Soluble in Ethanol, Chloroform and ethyl Ether. This medication is Used to Relieve Pain And itching from Certain Ear Conditions. Benzocaine is a Topical Anesthetic that Helps to Numb the Pain and Itching. Benzocaine is Indicated to Treat a Variety of Pain-related Conditions. It May Be Used for Local Anesthesia of Oral and Pharyngeal Mucous Membranes (sore Throat, Cold Sores, Mouth Ulcers, Toothache, Sore Gums, Denture Irritation, Otic Pain (earache), Surgical or Procedural Local Anesthesia.
Ramipril is a long-acting angiotensin-converting enzyme inhibitor. It is a prodrug that is transformed in the liver to its active ramiprilat. Ramipril is an angiotensin converting enzyme inhibitor. The mechanism of action of ramipril is as an angiotensin-converting enzyme inhibitor. Ramipril is a prodrug and nonsulfhydryl angiotensin converting enzyme (ace) inhibitor with antihypertensive activity. Ramipril is converted in the liver by de-esterification into its active form ramiprilat, which inhibits ace, thereby blocking the conversion of angiotensin I to angiotensin ii. This abolishes the potent vasoconstrictive actions of angiotensin ii & leads to vasodilatation. This agent also causes an increase in bradykinin levels and a decrease in angiotensin ii-induced aldosterone secretion by the adrenal cortex, thereby promoting diuresis and natriuresis.
Allopurinol is axanthine oxidase inhibitor that decreases uric acid production. It also acts as an antimetabolite on some simpler organisms. Allopurinol is a xanthine oxidase inhibitor. The mechanism of action of allopurinol is as a xanthine oxidase inhibitor. Allopurinol is a structural isomer of hypoxanthine. Allopurinol inhibits xanthine oxidase, an enzyme that converts oxypurines to uric acid. By blocking the production of uric acid, this agent decreases serum and urine concentrations of uric acid, thereby providing protection against uric acid-mediated end organ damage in conditions associated with excessive production of uric acid, i.e. The massive cell lysis associated with the treatment of some malignancies.