Our Products
Our Complete range of products are Mometasone Furoate Monohydrate and Tropicamide.
Mometasone Is A Medium-potency Synthetic Corticosteroid With Antiinflammatory, Antipruritic And Vasoconstrictive Properties. Mometasone Provides A Favorable Ratio Of Topical To Systemic Activity Due To Its Primary Local Effect Along With The Extensive Hepatic Metabolism And The Lack Of Active Metabolites. Though It Is Effective For Treatment Of Asthma, Glucocorticoids Do Not Affect Asthma Symptoms Immediately. Maximum Improvement In Symptoms Following Inhaled Administration Of Mometasone Furoate. 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. Mometasone Furoate Is Used In The Treatment Of Inflammatory Skin Disorders (Such As Eczema And Psoriasis)(Topical Form) , Allergic Rhinitis (Topical Form) (Such As Hay Fever), Asthma (Inhalation Form) For Patients Unresponsive To Less Potent Corticosteroids And Penile Phimosis. In Terms Of Steroid Strength, It Is More Potent Than Hydrocortisone And Less Potent Than Dexamethasone.
Details
Paracetamol (Acetaminophen) Is Used To Treat Many Conditions Such As Headache, Muscle Aches, Arthritis, Backache, Toothaches, Colds And Fevers. Paracetamol Is Widely Used Over The Counter. It Is Commonly Used To Help With Headaches, Other Minor Aches And Pains, And Is A Major Ingredient In Many Cold Medications. In Combination With Opioid Analgesics, Paracetamol Is Used In The Management Of More Severe Pain Such As Post-surgical And Cancer Pain. Though Paracetamol Is Used To Treat Inflammatory Pain, It Is Not Classified As An Nsaid Because It Exhibits Only Weak Anti-inflammatory Activity. Paracetamol Is Not Considered Carcinogenic At Therapeutic Doses. It Is Classified As A Mild Analgesic. It Is Also Used As An Intermediate For Pharmaceuticals(As A Precursor In Penicillin) And Azo Dyes, Stabilizer For Hydrogen Peroxide, Photographic Chemicals.
Details
Clopidogrel is a Platelet Aggregation Inhibitor. It Works By Slowing or Stopping Platelets from Sticking to Blood Vessel Walls or Injured Tissues. Clopidogrel is An Oral, thienopyridine-class antiplatelet Agent used to Inhibit Blood Clots In coronary Artery Disease, peripheral Vascular Disease, cerebrovascular Disease and to Prevent myocardial Infarction (heart Attack) and Stroke in People Who are At High Risk of These Events . the Drug Works By Irreversibly Inhibiting a Receptor Called p2y12, An Adenosine Diphosphate (adp) Chemoreceptor On Platelet Cell Membranes. Adverse Effects Include bleeding, Severe neutropenia, Andthrombotic Thrombocytopenic Purpura. It is also Used With aspirin to Treat New/worsening chest Pain (new heart Attack, Unstable angina) and to Keep blood vessels Open and Prevent blood Clots after Certain Procedures (such as Cardiac stent). Clopidogrel Works By Blocking Platelets from Sticking Together and Prevents Them from Forming Harmful Clots. It is An Antiplatelet Drug. It Helps Keep Blood Flowing Smoothly in Your Body.
Details :
Turmeric is A diarylheptanoid. About Two Centuries Ago, Isolation of a “yellow Coloring-matter” from the Rhizomes of Curcuma Longa (turmeric) & Was Named Curcumin. Turmeric's other Two Curcuminoids are Desmethoxycurcumin and bis-desmethoxy- Curcumin. the Curcuminoids Are natural Phenols that are Responsible for the Yellow Color of Turmeric. Curcumin Can Exist in Several Tautomeric forms, Including a 1, 3-diketo form and Two Equivalent Enol Forms. the Enol Form is More Energetically Stable in the Solid Phase and in Organic Solvents, While in Water the 1, 3-diketo dominates. Curcumin Can Be Used For boron Quantification in the Curcumin Method. It Reacts With boric Acid to Form a Red-color Compound, Rosocyanine. Curcumin is a Bright-yellow Color Powder and May Be Used as A food Coloring. Curcumin is Powerful Anti-inflammatory Effects and is a Very Strong Antioxidant. Combat Cancer Stem Cells and Enhance Heart Health and Inhibit the Formation of Ldl (bad) Cholesterol.
Details :
Esomeprazole is A proton Pump Inhibitor Others Worldwide Which Reduces Stomach Acid secretion Through Inhibition of The h+/k+ atpase in The parietal Cells of the Stomach. By Inhibiting the Functioning of this Transporter, the Drug Prevents Formation of Stomach Acid. It is Used in the Treatment Of dyspepsia, peptic Ulcer Disease, gastroeso- Phageal Reflux Disease, And zollinger-ellison Syndrome. the Primary Uses of Esomeprazole are Treatment and Maintenance Of erosive Esophagitis, Treatment Of duodenal Ulcers caused By h. Pylori, Prevention Of gastric Ulcers in Those On Chronic nsaid therapy, and Treatment of Gastrointestinal Ulcers Associated With crohn's Disease. It Works By Decreasing the Amount of Acid Your Stomach Makes. It Relieves Symptoms such As heartburn, Difficulty Swallowing, and Persistent cough. This medication helps Heal Acid Damage to the Stomach and Esophagus, Helps Prevent Ulcers, and May Help Prevent cancer of the Esophagus.
Details
Artesunate is a water-soluble, semi-synthetic derivative of the sesquiterpine lactone artemisinin with anti-malarial, anti-shistosomiasis, antiviral, and potential anti-neoplastic activities. Upon hydrolysis of artesunate's active endoperoxide bridge moiety by liberated heme in parasite-infected red blood cells, reactive oxygen species and carbon-centered radicals form, which have been shown to damage and kill parasitic organisms. Additionally, in vitro studies demonstrate that this agent induces dna breakage in a dose-dependent manner. Artesunate has also been shown to stimulate cell differentiation, arrest the cell cycle in the g1 and g2m phases, inhibit cell proliferation, and induce apoptosis through mitochondrial and caspase signaling pathways. Artemisinin is isolated from the plant artemisia annua. Artesunate is part of the artemisinin group of drugs that treat malaria. It is a semi-synthetic derivative of artemisinin that is water-soluble and may therefore be given by injection.
Additional Information:
Payment Terms : L/C, T/T
Packaging Details : OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS
Delivery Time : 2 - 4 WEEKS
Additional Information:
Packaging Details : OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS
Delivery Time : 2 - 4 WEEKS
We are Offering Various Types of Antioxidants like Tbhq (tertiary Butyl Hydroquinone), Bha (butylated Hydroxy Anisole), Bht (butylated Hydroxy Toluene) Etc. We Can also Supply other Antioxidants On Specific Demand.
TBHQ a Highly Effective antioxidant in Foods, Used as A preservative for Unsaturated vegetable Oils and Many Edible Animal Fats. It Can Be Combined with other Preservatives such As bha. Its Primary Advantage is Enhancing Storage Life. Synonyms: 2-tert-butylbenzene-1, 4-diol – Cas Number: 1948-33-0, Mol. Formula: C10h14o2, Mol. Weight: 166.22. It is White Crystalline Powder with Its Melting Range of 126°C -129°C. It is Insoluble in Water.
BHA (butylated Hydroxy Anisole) is An antioxidant consisting of a Mixture of Two isomeric organic Compounds, 2-tert-butyl-4-hydroxyanisole and 3-tert-butyl-4-hydroxyanisole. It is a Waxy Solid Used as Food Additive, Antioxidant & Preservative in Food, Food Packaging, Animal Feed, Cosmetics, Rubber, and Petroleum Products. bha also is Commonly Used in Medicines, such As isotretinoin, Lovastatin, And simvastatin, among Others. Synonyms: 2-tert-butyl-4-methoxyphenol;3-tert-butyl-4-methoxyphenol-– Cas Number: 25013-16-5, Mol. Formula: C11h16o2, Mol. Weight: 180.24. It is White to Slightly Yellowpowder with Its Melting Range of 48°c -55°c. It is Insoluble in Water.
BHT (butylated Hydroxytoluene), also Known As dibutylhydroxytoluene, Useful for Its antioxidant properties. It is Used as Food Additive, Household Product Ingredient, Industrial Additive, Personal Care Product/cosmetic Ingredient, Pesticide Ingredient, Plastic/rubber Ingredient and Medical/veterinary/research.
Details :
Amlodipine Besylate is a Long-acting Dihydropyridine Calcium Channel Blocker. It is Effective in the Treatment of Angina Pectoris and Hypertension. Amlodipine is Used with or Without Other medications to Treat high Blood Pressure. Lowering high Blood Pressure helps Prevent Strokes, heart Attacks, And kidneyproblems. Amlodipine Belongs to a Class of Drugs Known As calcium channel Blockers. It Works By Relaxing blood vessels So blood can Flow More Easily. Amlodipine is also Used to Prevent Certain Types Of chest Pain (angina). It May Help to Increase Your Ability To exercise and Decrease the Frequency of Angina Attacks. It Should Not Be Used to Treat Attacks of Chest Pain When They Occur.
Details :
Pemetrexed Disodium Is Approved To Be Used Alone Or With Other Drugs To Treat Malignant Pleural Mesothelioma In Patients Who Cannot Be Treated Withsurgery. Non-small Cell Lung Cancer (Certain Types) In Patients Whose Disease Is Locally Advanced Or Has Metastasized (Spread To Other Parts Of The Body).pemetrexed Disodium Is Also Being Studied In The Treatment Of Other Types Ofcancer. Its Indications Are The Treatment Of Non-small Cell Lung Cancer And Pleural Mesothelioma. Pemetrexed Is In A Class Of Medications Called Antifolate, Antineoplastic Agents And Antimetabolite For Ts, Dhfr And Garft With Ki Of 1.3 Nm, 7.2 Nm And 65 Nm, Respectively. It Works By Blocking The Action Of A Certain Substance In The Body That May Help Cancer Cells Multiply.
Details
It Is Beta-amino Acid-derived Inhibitor Of Dipeptidyl Peptidase 4 (Ddp-4) With Hypoglycemic Activity. Sitagliptin Phosphate Is A Pyrazine-derived Dipeptidyl-peptidase Iv Inhibitor And Hypoglycemic Agent That Increases The Levels Of The In Cretin Hormones Glucagon-like Peptide-1 (Glp-1) And Glucose-dependent Insulinotropic Polypeptide (Gip). Sitagliptin Is The First In A New Class Of Once Daily, Oral Anti-hyperglycaemic Agents. When Added To Ongoing Metformin Or Pioglitazone Therapy, It Significantly Improved Hba1c In Type-2 Diabetic Patients Who Failed To Achieve Adequate Glycaemic Control With These Agents As Monotherapy And It Was Found To Be Non-inferior To Glipizide When Added To Metformin. This Enzyme-inhibiting Drug Is Used Either Alone Or In Combination With Other Oral Antihyper- Glycemic Agents (Such As Metformin Or A Thiazolidinedione) For Treatment Of Diabetes Mellitus Type 2. The Benefit Of This Medicine Is Its Fewer Side Effects (E.g., Less Hypoglycemia, Less Weight Gain) In The Control Of Blood Glucose Values. While Safety Is Its Advantage, Efficacy Is Often Challenged As It Is Often Recommended To Be Combined With Other Agents Such As Metformin.
Details
Additional Information:
Payment Terms : L/C, T/T
Packaging Details : OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS
Delivery Time : 2 - 4 WEEKS
Cefixime is a third-generation cephalosporin antibiotic that is stable to hydrolysis by beta-lactamases. Cefixime, an antibiotic, is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result, many organisms resistant to penicillins and some cephalosporins due to the presence of beta-lactamases, may be susceptible to cefixime.the antibacterial effect of cefixime results from inhibition of mucopeptide synthesis in the bacterial cell wall.
Erythromycin is a macrolide and macrolide antimicrobial. The physiologic effect of erythromycin is by means of decreased sebaceous gland activity. The chemical classification oferythromycin is macrolides. A bacteriostatic antibiotic macrolide produced by streptomyces erythreus. Erythromycin a is considered its major active component. In sensitive organisms, it inhibits protein synthesis by binding to 50s ribosomal subunits. This binding process inhibits peptidyl transferase activity and interferes with translocation of amino acids during translation and assembly of proteins. Erythromycin is a broad-spectrum, macrolide antibiotic with antibacterial activity. Erythromycin diffuses through the bacterial cell membrane and reversibly binds to the 50s subunit of the bacterial ribosome. This prevents bacterial protein synthesis. Erythromycin may be bacteriostatic or bactericidal in action, depending on the concentration of the drug at the site of infection and the susceptibility of the organism involved.
Ibuprofen is a nonsteroidal anti-inflammatory agent with analgesic properties used in the therapy of rheumatism and arthritis. Ibuprofen is a propionic acid derivate and nonsteroidal antiinflammatory drug (nsaid) with anti-inflammatory, analgesic, and antipyretic effects. Ibuprofen inhibits the activity of cyclo-oxygenase I and ii, resulting in a decreased formation of precursors of prost- aglandins and throm- boxanes. This leads to decreased prostaglandin synthesis, by prost- aglandin synthase, the main physiologic effect of ibuprofen. Ibuprofen also causes a decrease in the formation of thromboxane a2 synthesis, by thromboxane synthase, thereby inhibiting platelet aggregation.
Additional Information:
Payment Terms : L/C, T/T
Packaging Details : OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS
Delivery Time : 2 - 4 WEEKS
Mecobalamin (mecobalamin, mecbl, or meb12) is a cobalamin, a form of vitamin b12. It differs from cyanocobalamin in that the cyanide is replaced by a methyl group. Methylcobalamin features octahedral cobalt (iii) centre. Methylcobalamin can be obtained as bright red crystals. From the perspective of coordination chemistry, methyl cobalamin is notable as a rare example of a compound that contains metal-alkyl bonds. Nickel-methyl intermediates have been proposed for the final step of methanogenesis. Mecobalamin is equivalent physiologically to vitamin b12, and can be used to prevent or treat pathology arising from a lack of vitamin b12 (vitamin b12 deficiency) such as pernicious anemia. Methylcobalamin is also used in the treatment of peripheral neuropathy, diabetic neuropathy & as a preliminary treatment foramyotrophic lateral sclerosis.
Additional Information:
Payment Terms : L/C, T/T
Packaging Details : OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS
Delivery Time : 2 - 4 WEEKS
Meloxicam is a nonsteroidal anti-inflammatory drug. The mechanism of action of meloxicam is as a cyclooxygenase inhibitor. The chemical classification of meloxicam is nonsteroidal anti-inflammatory compounds. Meloxicam is an oxicam derivative and a non-steroidal anti-inflammatory drug (nsaid) with anti-inflammatory, antipyretic and analgesic activities. Unlike traditional nonselective nsaids, meloxicam preferentially inhibits the activity of cyclo-oxygenase ii (cox-ii), resulting in a decreased conversion of arachidonic acid into prostaglandin precursors. The resulting decrease in prostaglandin synthesis is responsible for the therapeutic effects of meloxicam.
Additional Information:
Payment Terms : L/C, T/T
Packaging Details : OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS
Delivery Time : 2 - 4 WEEKS
Additional Information:
Payment Terms : L/C, T/T
Packaging Details : OFFERED IN EXPORT WORTHY PACKING OF 25 KILOS OR AS PER OUR CUSTOMER REQUIREMENTS
Delivery Time : 2 - 4 WEEKS