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Adenosine Injection

Adenosine Injection
  • Adenosine Injection
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  • It is physiological substance present normally in the body. It is one of the drug of choice for paroxysmal supraventricular tachycardia.
Composition : 6mg/2ml, 30mg/10ml
Indications : Treatment of PSVT. Diagnosis ofre-entrant atrial and ventricular tachycardia.
Contraindications :Various degrees of heart block, sicksinus syndrome and bronchial asthma .
Safety Profile : In patients of atrialflutter/fibrillation, in pregnancy used if absolute necessary.
Adverse Effects :Flushing, dyspnoea, nausea, lightheadedness, sweating, palpitation & heaviness in arms.
Dosage :Adults - initial dose of 3.5mg asrapid intravenous bolus, second dose is repeated after 2 mts, if firstdose fails to abort the attack of PSVT. It is given 6mg rapidlyintravenously, If attack still persists, give third dose of 12mg rapidlyintravenously. Additional or higher doses are not recommended.
Purity :Not less than 99%.
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Alpha Beta Arteether Injection

Alpha Beta Arteether Injection
  • Alpha Beta Arteether Injection
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  • It is synthetic derivative of artemisinin, a product of chinses palnt, artemesi aannua. It is fast acting blood schizontocidal agent for P.falciparum malaria at the erythrocytic stage.
Composition :150mg/2ml
Indications :Chloroquine resistant malaria, complicated falciparam malaria and cerebral malaria .
Purity :Not less than 99%.
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Analgin Injection

Analgin Injection
  • Analgin Injection
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  • It is a derivative of Pyrazolone having analgesic and antipyretic activity.
Composition :1mg/2ml, 15mg/30ml
Indications :Pain, Fever.
Contraindications:Hypersensitivity,hepatic porphyria,Collapse states, infants less than 3 month of age or 5kg body wt.
Safety Profile :Disorders of haematopoiesis.
Adverse Effects :Hypersensitivity,bronchial tract, gastric symptoms.
Drug InteractionsCyclosporine level increased.
Dosage :Adults : Oral ; 0.5-1.5gm in 2-3divided doses. Parenteral : 2ml IM. 2-3 times daily.Children : Oral 30-60 mg/kg/day
Parenteral (All four times/day by slow IV) : 3 month to 1 year : 0.1ml, below 5 years : 0.2ml, 5-7 years : 0.4ml, 8-11 years : 0.5ml, 12-14 years : 0.8ml
Purity :Not less than 99%.
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Anti Biotic Capsules

Anti Biotic Capsules
  • Anti Biotic Capsules
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  • Amoxycillin250mg, 500mg
    Amoxycillin Bromhexine 250mg 8mg
    Amoxycillin Bromhexine LB 250mg 8mg 60 million spores
    Amoxycillin Carbocisteine 500mg 150mg
    Amoxycillin Cloxacillin 250mg 250mg
    Amoxycillin Cloxacillin LB250mg 250mg 60 million spores
    Amoxycillin Dicloxacillin 250mg 250mg
    Ampicillin250mg, 500mg
    Ampicillin Cloxacillin 250mg 250mg
    Azithromycin 250mg
    Cefaclor 500mg
    Cefadroxil 250mg, 500mg
    Cefdinir 300mg
    Cefixime Clavulanic Acid 100mg 62.5mg, 200mg 125mg
Cefixime Cloxacillin 100mg/ 200mg 500mg
Ceftibuten400mg
Cephalexin 250mg, 500mg
Cloxacillin 250mg, 500mg
Erythromycin 250mg
Lincomycin 500mg
Vancomycin 125mg
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Anti Microbial Capsules

Anti Microbial Capsules
  • Anti Microbial Capsules
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  • COMPOSITION :- 
  • Chloramphenicol250mg, 500mg
    Doxycycline100mg
    Minocycline50mg, 100mg
    Oxytetracycline250mg
    Tetracycline250mg, 500mg
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Artemether Injection

Artemether Injection
  • Artemether Injection
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  • Composition :80mg/1ml
    Indications :Chloroquine sensitive, chloroquine resistant and multidrug resistant falciparum malaria & severe malaria including cerebral malaria.
    Contraindications :Patient with cardiac problems and pregnancy for longer use.
    Safety Profile :Drugs known to produce heart block or prolong QT interval should be avoided while artemether is being administer. 1st trimester of pregnancy is contraindication for its use.
    Adverse Effects :Nausea, vomiting, abdominal pain, bradycardia, first degree heart block, transient increase in transaminases, reversible decrease in reticulocyte count.
    Dosage :A 5-day dose scheme is followed 80mg .m. Twice a day on day one, followed by 80mg i.m. Once a day for follow.
    Purity :Not less than 99%.
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Bleomycin Injection

Bleomycin Injection
  • Bleomycin Injection
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  • Category: anti-neoplastic. Each vial contains:-Bleomycin sulphate -15 units, 30 units. Bleomycin sulfate for injection is a mixture of cytotoxic glycopeptide antibiotics isolated from strain of streptomyces verticillus. It is freely soluble in water. Between 4. 5 to 6. 0
Pharmacological Action : Bleomycin is a mixture of cytotoxic glycopeptide antibiotics. It inhibits DNA synthesis. When administered intrapleurally, bleomycin acts as a sclerosing agent.
Precautions: Bleomycin be administered under the supervision of a qualified health care provider experienced in the use of cancer chemotherapeutic agents. Appropriate management of therapy and complications is possible only when adequate diagnostic and treatment facilities are readily available. Before using Bleomycin Sulfate for injection medication, tell your doctor or pharmacist your medical history, especially: immune system problems (e.g., chemotherapy, bone marrow problems), kidney disease, liver disease, lung problems.
Indications:Bleomycin Sulfate Injection should be considered a Palliative Treatment. It has been shown to be useful in the management of the following neoplasms either as a single agent or in proven combinations with other approved
chemotherapeutic agents: Squamous Cell Carcinoma in Head and neck including mouth, tongue, tonsil, Nasopharynx, Oropharynx, Sinus, palate, Lip, Buccal Mucosa, Gingivae , Epiglottis, skin, Larynx, Cervix, and Vulva. Lymphomas, Testicular Carcinoma, Malignant Pleural Effusion.
Contraindications : Bleomycin Sulfate injection is contraindicated in patients who have demonstrated a hypersensitive or an idiosyncratic reaction to it.
Adverse Effects : Pneumonitis progressing to pulmonary anaphylactoid reactions, erythema, rash, striae, vesiculation, hyperpigmentation, rarely myocardial infarction, cerebrovascular accident, haemolytic uraemia syndrome, cerebral arthritis.
Local reactions : Pain, pruritus, hyperpigmentation, scarring, suppuration scaling.
Dosage :Bleomycin Sulfate injection may be given by the Intramuscular, intravenous, subcutaneous, or Intrapleural routes. Squamous cell carcinoma, non-Hodgkin's lymphoma, testicular carcinoma- 0.25 to 0.50 units/kg (10 to 20 units/m�) given intravenously, intramuscularly, or subcutaneously weekly or twice weekly.
Hodgkin's disease:- 0.25 to 0.50 units/kg (10 to 20 units/m�) given intravenously, intramuscularly, or subcutaneously weekly or twice weekly.
Note: When Bleomycin sulfate injection is used in combination with other antineoplastic agents, pulmonary toxicities may occur at lower doses.
Malignant Pleural Effusion - 60 units administered as a single dose Bolus Intrapleural Injection.
Intramuscular or Subcutaneous: Bleomycin Sulfate injection 15 units vial should be reconstituted with 1 to 5 ml of Sterile Water for Injection, Sodium Chloride for Injection 0.9% or Sterile Bacteriostatic Water for Injection. Bleomycin Sulfate injection 30 units vial should be reconstituted with 2 to 10 ml of the above diluents.
Intravenous: The contents of the 15 units or 30 units vial should be dissolved in 5 ml or 10 ml, respectively, of Sodium Chloride for Injection, 0.9% and administered slowly over a period of 10 minutes.
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Cardiovascular Tablets

Cardiovascular Tablets
  • Cardiovascular Tablets
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  • Our customers can avail Cardiovascular Tablets from us. The offered range of cardiovascular tablets is processed utilizing optimum grade ingredients, sourced from dependable vendors of the market. Along this, the offered range of cardiovascular tablets of dining chair is tested on different parameters to maintain its authenticity throughout the formulation process.

Features:

  • Safe to consume
  • Hygienically packed
  • Longer shelf life
Amiloride Hydrochlorothiazide5mg 50mg
Amiodarone100mg, 200mg
Amlodipine2.5mg, 5mg, 10mg
Amlodipine Atenolol5mg 50mg, 5mg 25mg
Amlodipine Enalapril5mg 5mg
Atenolol50mg, 100mg
Atenolol Nifedipine50mg 20mg
Atorvastatin10mg, 20mg
Chlorthalidone100mg
Clonidine100mcg, 150mcg
Labetalole100mg
Losartan Potassium25mg, 50mg
Losartan Potassium Amlodipine50mg 5mg, 25mg 5mg
Losartan Potassium Hydrochlorothiazide50mg 12.5mg
Nebivolol S-Amlodipine Besylate5mg 2.5mg
Nifedipine10mg, 20mg
Olmesartan Amlodipine20mg 5mg
Prazosin2.5mg
Propranolol10mg, 40mg, 80mg
Quinidine200mg, 300mg
Ramipril2.5mg, 5mg
Ramipril Hydrochlorothiazide2.5mg 12.5mg, 5mg 12.5mg
Reserpine0.25mg
Telmisartan20mg, 40mg
Telmisartan Hydrochlorothiazide40mg 12.5mg
Verapamil40mg, 80mg

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Cefoperazone And Sulbactum Injection

Cefoperazone And Sulbactum Injection
  • Cefoperazone And Sulbactum Injection
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Product Details:

Medicine TypeAllopathic

  • Cefoperazone is third generation cephalosporin antibacterial component of Cefoperazone Sodium and Sulbactam Sodium, which acts against sensitive during the stage of active multiplication by inhibiting biosynthesis of cell wall mucopeptide. The combination has a broader spectrum of activity.
Composition : 0.5gm 0.5gm, 1gm 1gm
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Daunorubicin Injection

Daunorubicin Injection
  • Daunorubicin Injection
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  • It is an anthracycline cytotoxic antibiotic produced by a strain of streptomyces peucetius. It inhibits the synthesis of nucleic acids and effects on DNA & particularly rapid and marked.
Composition : 20mg
Indications : Remission indication in non lymphocytic leukemia, acute erythroid, leukemia, acute monocytic, leukemia, acute myelogenous leukemia, acute Lymphoblast
Contraindications :Pre- existing drug induced bone marrow supression, pre-existing heart disease, pregnancy.
Safety Profile : Cardiac, renal & hepatic functions adn serum uric levels should be evaluated prior to treatment. Completed blood count should be frequently monitored during the therapy extravasation at site of injections may causes severe local tissue necrosis.
Adverse Effects :Myelosuppression, myocardial toxicity, infants and children's are more susceptible to congestive heart failure (CHF), reversible alopecia gastrointestinal
A special preparation as daunorubicin citrate liposome contain an equal amount of citrate encapsulated in lipid vesicles, formulated to maximize the selectivity of the drug for soiled tumors in sites.
Drug Interactions :1st line drug for advanced HIV associated keposi's saecoma.
Dosage :Acute nonlymphocytic leukemia: Less than 60 years age -45 mg/m²/day i.v on days 1,2,3 on first course and on day 1&;2 on subsequent course with cytosine.
Acute Lymphocytic leukemia (All): Chlidren 25 mh/ m² i.v on day every week with prednisolone and vincristine.In < 2yrs of age: mg/kg dose in same manner Adult: 45 mg/m²per day i.v on drug 1,2,3 with vincristine., prednisolone and L-asparaginase.
In < 2yrs of age: mg/kg dose in same manner Adult: 45 mg/m²per day i.v on drug 1,2,3 with vincristine., prednisolone and L-asparaginase.
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Diabetic Tablets

Diabetic Tablets
  • Diabetic Tablets
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  • In order to cater to the diverse requirements of esteemed clients, we are able to offer an unparalleled assortment of Diabetic Tablets. The offered range is formulated utilizing premium grade ingredients, sourced from trustworthy vendors of the market. Along with this, the offered assortment is tested utilizing highly stringent procedures to maintain its authenticity throughout the formulation process.

Features:

  • Precise pH value
  • Accurate composition
  • Longer shelf life

Gliclazide Metformin (ER)80mg 500mg
Glibenclamide Metformin (ER)5mg 500mg
Glimepiride1mg, 2mg
Glimepiride Metformin (ER)1mg,2mg 500mg
Glimepiride Pioglitazone Metformin (ER)1mg/2mg 15mg 500mg
Metformin (ER)500mg
Pioglitazone15mg,30mg


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Fludarabine Injection

Fludarabine Injection
  • Fludarabine Injection
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  • Category: Anti-neoplastic
Each lyophilized vial contains:- Fludarabin 50 mg
Fludarabine phosphate is rapidly dephosphorylated to 2-fluoro-ara-A and then phosphorylated intracellularly by deoxycytidine kinase to the active triphosphate, 2-fluoro-ara-ATP. This metabolite appears to act by inhibiting DNA polymerase alpha, ribonucleotide reductase and DNA primase, thus inhibiting DNA synthesis. The mechanism of action of this antimetabolite is not completely characterized and may be multi-faceted.
Specification-pH: 6.0 ­ 7.1
Indication :Fludarabine is primarily indicated in conditions like Chronic lymphocytic leukaemia,Lymphoid malgnancies, and can also be given in adjunctive therapy as an alternative drug of choice in Acute leukemia, Indolent lymphoma, Myclodysplastic syndrome, Myelodysplastic syndrome, Myeloid leukaemia.
Dosage :-The recommended adult dose of fludarabine for injection is 25 mg/m² administered intravenously over period of approximately 30 minutes daily for five consecutive days. Each 5 day course of treatment should commence every 28 days.
Contra Indications:-Fludarabine is contraindicated in conditions like Peripheral neuropathy, HIV infection, Renal impairment, Central neuropathy.
Precautions:-During and after treatment with fludarabine for injection, vaccination with live vaccines should be avoided. If it is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to the fetus. Women of childbearing potential should be advised to avoid becoming pregnant.
Drug interaction: The use of Fludarabin for injection in combination with pentostatin is not recommended due to the risk of severe pulmonary toxicity.
Storage:Store in refrigerator. Use within 8 hrs if kept at room temperature.
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Fludarabine Injection

Fludarabine Injection
  • Fludarabine Injection
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  • Category: Anti-neoplastic. Composition- : Each lyophilized vial contains :- Fludarabin - 50 mg, Fludarabine phosphate is rapidly dephosphorylated to 2-fluoro-ara-A and then phosphorylated intracellularly by deoxycytidine kinase to the active triphosphate, 2-fluoro-ara-ATP. This metabolite appears to act by inhibiting DNA polymerase alpha, ribonucleotide reductase and DNA primase, thus inhibiting DNA synthesis. The mechanism of action of this antimetabolite is not completely characterized and may be multi-faceted.
Specification-pH: 6.0 ­ 7.1
Indication :Fludarabine is primarily indicated in conditions like Chronic lymphocytic leukaemia,Lymphoid malgnancies, and can also be given in adjunctive therapy as an alternative drug of choice in Acute leukemia, Indolent lymphoma, Myclodysplastic syndrome, Myelodysplastic syndrome, Myeloid leukaemia.
Dosage :-The recommended adult dose of fludarabine for injection is 25 mg/m² administered intravenously over a period of approximately 30 minutes daily for five consecutive days. Each 5 day course of treatment should commence every 28 days.
Contra Indications:-Fludarabine is contraindicated in conditions like Peripheral neuropathy, HIV infection, Renal impairment, Central neuropathy.
Precautions:-During/after treatment with fludarabine for injection, vaccination with live vaccines should be avoided. If it is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to the fetus. Women of childbearing potential should be advised to avoid becoming pregnant.
Drug interaction: The use of Fludarabin for injection in combination with pentostatin is not recommended due to the risk of severe pulmonary toxicity.
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Gastro Intestinal Capsules

Gastro Intestinal Capsules
  • Gastro Intestinal Capsules
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Dicyclomine Paracetamol20mg 500mg
Digestive Enzymes100mg
Esomeprazole Domperidone 40mg 30mg
Lansoprazole15mg, 30mg
Multivitamins Lactobacillus 20mg
Omeprazole20mg
Omeprazole Domperidone 20mg 10mg
Pantoprazole Domperidone (SR) 40mg 30mg
Piracetam400mg
Rabeprazole Diclofenac20mg 100mg
Rabeprazole Domperidone (SR) 20mg 30mg
Racecadotril 100mg
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Irinotecan Injection

Irinotecan Injection
  • Irinotecan Injection
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  • Category: Anticancer. Each vial contains:- Irinotecan 40mg/2ml, 100mg/5ml. Specifications: Irinotecan injection is supplied as sterile, pale yellow, clear, aqueous solution. The pH of the solution is in between 3.0 to 3.8.
Composition : Each vial contains:
Irinotecan 40mg/2ml, 100mg/5ml Water for Injection q.s.
Indications : It is indicated as a component of first-line therapy in combination and leucovorin for patients with metastatic carcinoma of the colon or rectum.
It is also indicated for patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following initial fluorouracil-based therapy.
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Contraindications : It is contraindicated in patients with a known hypersensitivity to the drug or its excipients.
Pharmacological action: Irinotecan is a derivative of camptothecin. It interact specifically with the enzyme topoisomerase I which relieves torsional strain in DNA by inducing reversible single-strand breaks. Irinotecan and its active metabolite SN-38 bind to the topoisomerase I-DNA complex and prevent religation of these single-strand breaks.
Adverse Effects : : Abdominal discomfort, diarrhoea, Leukopenia, neutropenia, haemorrhage, body pain, insomania, dizziness, anaemia vomiting, nausea
Dosage : Irinotecam should be administered as an intravenous infusion over 90 minutes for both the weekly and once-every-3-week dosage schedules.
Weekly dose schedule: The usual starting dose is 125 mg/m2. Subsequent doses may be adjusted to as high as 150 mg/m2.
Once every three week schedule: starting dose is 350 mg.m2
Storage: 2-80C
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Leuprolide Injection

Leuprolide Injection
  • Leuprolide Injection
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  • Category: Anti-neoplastic, Composition- : Each 0.5ml Contains : Leuprolide Acetate 1mg
Specification-pH range – : 5.5 to 6.5
Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin releasing hormone (GnRH or LH-RH). The analog possesses greater potency than the natural hormone. It is a sterile, aqueous solution intended for subcutaneous injection.
Indication :Advanced prostatic carcinoma when orchidectomy or oestrogen administration is not indicated.
Dosage :-SC inj., 1 mg single dose.
Contraindications:-Pregnancy, in women who may become pregnant while receiving the drug, and during lactation. Sensitivity to benzyl alcohol (found in leuprolide injection). Undiagnosed abnormal vaginal bleeding. Hypersensitivity to GnRH/GnRH agonist analogs. The 30-mg depot in women.
Precautions:-Patients with metastatic vertebral lesions and/or with urinary tract obstruction should be closely observed during the first few weeks of therapy. Patients with known allergies to benzyl alcohol, an ingredient of the drug's vehicle, may present symptoms of hypersensitivity, usually local, in the form of erythema and induration at the injection site.
Drug interaction: Administration of leuprolide acetate in therapeutic doses results in suppression of the pituitary-gonadal system. Normal function is usually restored within 4 to 12 weeks after treatment is discontinued. Administration of leuprolide acetate in therapeutic doses results in suppression of the pituitary-gonadal system. Normal function is usually restored within 4 to 12 weeks after treatment is discontinued.
Adverse Effect-: High blood pressure, ischemia, insomnia, constipation, urinating more often than usual, bone pain, loss of movement in any part of your body; swelling, rapid weight gain.
Storage:: Store unopened bottles in the refrigerator. Vials can be kept at room temperature (less than 86 degrees F or 30 degrees C). Do not freeze. Protect from light.
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Mitoxantrone Injection

Mitoxantrone Injection
  • Mitoxantrone Injection
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Product Details:

Form of MedicineInjection
UsageCommercial

  • It is a synthetic antineoplastic anthracenedione for intravenous use. Although its mechanism of action is not fully elucidated, it is DNA - reactive agent. It has a cytocidal effect on with proliferating and non proliferating cultured small cells suggesting lock of cell cycle specifically.
Composition : Each ml contains:
Mitoxantrone 2 mg
Indications : It is used in the treatment of metastatic breast cancer and of non-Hodgkin's lymphomas, alone or with other agents. It may also be given to treat adult acute myeloid leukemia. Mitoxantrone has also been used in patients with hormone-refractory prostate cancer, liver cancer, and ovarian cancer. In addition, mitoxantrone is used in the management of secondary progressive or relapsing multiple sclerosis, to reduce neurological disability or the frequency of relapses.

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Contraindications : Mitoxantrone for injection is contraindicated in patients who have demonstrated prior hypersensitivity to it.
Adverse Effects : Serious adverse reactions including anaphylaxis and allergic reactions, neuropathy,pulmonary toxicities and hepatotoxicities can occur..
Dosage : In the treatment of breast cancer, prostate cancer, liver cancer, and lymphomas, a dose equivalent to mitoxantrone 14 mg/m2 is given initially and then repeated every 3 weeks. It is diluted to at least 50 ml in sodium
chloride 0.9% 5% and injected over at least 3 minutes into a freely-running intravenous infusion of
either. Subsequent doses may be adjusted according to the degree of Myelosuppression produced. Initial dosage
may need to be reduced to 12 mg/m2 in debilitated patients or those who have had previous Hemotherapy.
Precautions: Special Populations in Carcinogenesis, Mutagenesis, Impairment of Fertility, Hepatic Impairment, Pregnancy, Nursing Mothers, Pediatric Use, Geriatric Use, Multiple Sclerosis, Hormone-Refractory Prostate Cancer, Acute Nonlymphocytic Leukemia.
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Moxifloxacin Drop

Moxifloxacin Drop
  • Moxifloxacin Drop
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Pack Size : 5ml/10ml
Indications:- Conjunctivitis caused by susceptible strains of the Aerobic gram –positive microorganisms, Aerobic gram- negative microorganisms and other microorganisms.
Dosage:Instill one drop in the affected aye 3 times a day for 7 days.
Contra Indications:Hypersensitivity.
Special Precautions:Prolonged use result in overgrowth of non-susceptible organisms, including fungi. If superinfection occurs, discontinue use and institute alternative therapy.
Side-Effects: Decreased visual acuity, dry eye, keratitis, ocular discomfort, ocular hyperemia, ocular pain, ocular prurtius, sub- conjunctival hemorrhage, and tearing. Pregnancy , Nusing Mother , pediatric use.
Purity :Not less than 99%.
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Musculo Skeletal Capsules

Musculo Skeletal Capsules
  • Musculo Skeletal Capsules
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  • COMPOSITION :- 
  • Celecoxib100mg, 200mg
    Ciclesonide160mcg, 320mcg
    Diacerein 50mg
    Glucosamine Sulphate 100mg, 750mg
    Indomethacin25mg, 50mg
    Ketoprofen50mg
    Nimesulide Serratiopeptidase100mg 10mg
    Piroxicam20mg
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Piroxicam Injection

Piroxicam Injection
  • Piroxicam Injection
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Piroxicam: Its anti- inflammatory potency is similar to indomethacin and analgesic action is greater than aspirin. It has useful antipyretic proerty.
Indications:Its anti- inflammatory potency is similar to indomethacin and analgesic action is greater than aspirin. It has useful antipyretic proerty.
Dosage:Rheumatod arthritis, osteroarthritis, ankylosing, Spondylitis: 20mg daily as single dose. Maint : 10-30 mg .Acute Musculo-skeletal disorders: 40mg in a single or divided doses for 7-14 days. Acute gout : 40 mg as a single dose. Maint : 40 mg in single or divided doses for 4-6 days.
Contra-Indications:Hypersensitivity , pregnancy children patients who develop asthama or allergy with other inflammatory drugs, lactation.
Special Precautions:Renal or hepatic dysfunction, asthma surgery, haemorrhagic disorders. Hypertension. Cardiovascular disease.
Paediatrics: Not recommended in age below 6 yrs.
Pregnancy:Contraindicated may affect the foetus.
Lactation:Safety not established.
Elderly:Reduced dose necessary.
Side Effects: Heart burn, nausea, anorexia, rashes, pruritus, C.N.S. manifestations. Oedema.
Drug Interactions: Potentiate anticoagulants. Diuretics increase risk of renal damage. Monitor lithium levels. Aspirin reduces serum levels.
Purity :Not less than 99%.
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Sparfloxacin Drop

Sparfloxacin Drop
  • Sparfloxacin Drop
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Pack Size : 10ml
Category: Antiinfective
Indications: In eye : Treatment of bacterial conjunctivitis, bacterial corneal infections like keratitis, kerato- conjunctivitis and conrneal ulcer caused by susceptible microorganisms.In ear treatment of otitis externa and otitis media with discharges due to susceptible microorganisms.
Dosage:In eye : Instill 1-2 drops in the affected eye (s) once ever 2-3 hours. The frequency can be adjusted based on the severity of infection.In ear : Instill 1-2 drops in the effected external ear (s) 3-4 times.
Contraindications:1 drop into the lower conjunctival sac 2-3 times daily. Duration of treatment : 7-9 days.
Special Precautions:Should irritation or hypersensitivity to any comoonent of drug develop, discontinue use of the preparation and institute appropriate therapy. Safety in pregnant and lactating woman has not been established. Avoid use in growing children and adolescents.
Side Effects:Ocular tolerance studies in rabbits have not revealed any severe intolerance reaction. Some burning and irritation may occur after topical instillation in eye or ear.Sparfloxacin Eye Drop
Purity :Not less than 99%.
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Topotecan Injection

Topotecan Injection
  • Topotecan Injection
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  • Category: Antineoplastic
  • Each vial contains: Topotecan HCl equivalent to Topotecan 2.5mg/2.5ml, 4mg/4ml.
Specification-Light Greenish color powder filled in glass vials.
pH 2.5 to 4.5
Indication :Metastatic carcinoma of the ovary after failure of initial or subsequent chemo therapy. Small cell lung cancer disease after failure of first line chemotherapy
Dosage :-Recommended starting dose is 1.5mg/m2 body surface area by IV infusion over 30 minutes daily for 5 consecutive days In absence of tumor progression, a minimum of four courses are recommended, as tumour response may be delayed.
Contraindications:-Severe hypersensitivity reactions (e.g., anaphylactoid reactions)
Pregnant or Breastfeeding,
Severe bone marrow depression.
Precautions:-Bone Marrow Suppression, Thrombocytopenia, Diarrhea, Interstitial Lung Disease, Pregnancy Neutropenia, Thrombocytopenia, Anemia.
Drug interaction: Cyclosporine A (inhibitor of ABCB1, ABCC1 [MRP-1], and CYP3A4) with hycamtin capsules increased topotecan exposure to 2- to 3-fold of control. The pharmacokinetics of topotecan were generally unchanged when coadministered.
Adverse Effect-: Bone marrow suppression. Primarily neutropenia, thrombocytopenic anaemia, abdominal discomfort.
Storage:Store between 2-80C
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Levofloxacin Tablet

Levofloxacin Tablet
  • Levofloxacin Tablet
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Sparfloxacin Tablets

Sparfloxacin Tablets
  • Sparfloxacin Tablets
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Dacarbazine Injection

Dacarbazine Injection
  • Dacarbazine Injection
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Product Details:

UsageHospital

  • Category: Anti-neoplastic
Each lyophilized vial contains:- Dacarbazine USP 100mg/ 200 mg/ 500mg
It is an unidarole derivative. Exact machanism of action is not known. Three hypothesis have been proposed.
• Inhibition of DNA synthesis by acting as purine analogue.
• Action as an alkylating agent.
• Interaction with - SH group. pH ranges from 3.0 to 4

Indication :Dacarbazine for injection is indicated in the treatment of metastatic malignant melanoma. In addition, dacarbazine for injection is also indicated for Hodgkin's disease as a secondary-line therapy when used in combination with other effective agents.
Dosage :-Malignant melanoma : 2-4.5 mg/kg/day for 10 days may be repeated at 4 weeks intervel or 250 mg/ml of body surface area (BSA)/day for 5 days repeated after 3 weeks.
Contra Indications:-Dacarbazine for injection is contraindicated in patients who have demonstrated a hypersensitivity to it in the past.
Precautions:-Breast-feeding is usually stopped while using anticancer drugs. Dacarbazine should be used only when clearly needed during pregnancy.
Drug interaction:Impairs immune response to vaccines; possible infection after admin of live vaccines. Effect increased by CYP1A2 inhibitors e.g. amiodarone, ciprofloxacin, fluvoxamine, ketoconazole, lomefloxacin, ofloxacin and . Effect decreased by CYP1A2 inducers e.g. aminoglutethimide, carbamazepine, and rifampicin.
Adverse effects:Haemopoietic depression invading mainly leucocytes and platelets anaphylactoid reaction, anorexia, nausea, vomiting, diarrhoea, influneza like syndrome, alopecia, facial flushing, paresthesia, ash liver function and renal function abnormalities
Storage:Store in a refrigerator 2°C to 8°C (36°F to 46°F). dacarbazine Use within 8 hours of reconstitution. Protect from light
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