Health Biotech Limited
Health Biotech Limited
Sector 34, Chandigarh
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Pharmaceuticals Injections

Pioneers in the industry, we offer vinblastine injection, cefotaxime sulbactum injection, mitomycin injection, n-acetyl cysteine injection, vincristine injection and tobramycin injection from India.

Vinblastine Injection

Vinblastine Injection
  • Vinblastine Injection
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Product Details:

TypeAllopathic
Form of MedicineInjection
Medicine TypeAllopathic
UsageCommercial

Composition : Each vial contains
Vinblastin Sulphate USP 1.0mg

Indications : Vinblastine sulfate (vinblastine sulfate injection) is indicated in the treatment of the following:

- Frequently Responsive Malignancies
- Generalized Hodgkin's disease
- Lymphocytic lymphoma (nodular and diffuse, poorly and well differentiated)
- Histiocytic lymphoma
- Mycosis fungoides (advanced stages)
- Advanced carcinoma of the testis
- Kaposi's sarcoma
- Letterer-Siwe disease
- Less Frequently Responsive Malignancies
- Choriocarcinoma resistant to other chemotherapeutic agents
- Carcinoma of the breast, unresponsive to appropriate endocrine surgery and hormonal therap
Contraindications : Pregnancy. Granulocytopenia, Bacterial infections.
Adverse Effects : Hair loss, leucopenia, neuritic pain, constipation, sensory loss, paresthesias, difficulty in walking (stepping gait), loss of deep tendon reflexes, muscle wasting, fever, hypersensitivity reaction, polyuria, urinary retention, hypertension, hypotension, cranial nerve palsy, headache, bone pains, jaw pain, parotid pain, myalgia, convulsions, syndrome of inappropriate secretion of ADH..
Dosage : Given I.V. at weekly intervals. Children : 2mg/m2 (if <10kg, start with 0.005 mg/kg/week) adult : 1.4mg/m2. Decrease the dose to 50%, if S. bilirubin is >3mg/dl. Not given to patients getting radiation therapy through ports that includes liver.
Precautions: Toxicity may be enhanced in the presence of hepatic insufficiency.
- Acute uric acid nephropathy,
- Acute shortness of breath
severe broncospasm have been reported following the administration of vinca alkaloids.
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Cefotaxime Sulbactum Injection

Cefotaxime Sulbactum Injection
  • Cefotaxime Sulbactum Injection
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Product Details:

Product TypeFinished Product
Medicine TypeAllopathic
Usage/ApplicationCommercial

  • It is an anti-infective combination of Cefotaxime and Sulbactam. Cefotaxime is a broad-spectrum semi-synthic third generation cephalosporin with potent bactericidal activity against a wide range of gram-positive and gram-negative bacteria. Sulbactam is beta lactamase inhibitor.
Composition : 500mg 250mg, 1gm 0.5gm
Indications : LRTI, GIT infections.
Dosage :Adult : Mild to moderate : 1g/0.5g to 2g/1g of cefotaxime/sulbactam every 8-12 hours.
Moderate to severe : 1g/0.5g to 2g/1g of cefotaxime/sulbactam every 6-8 hours.
Children : 100/50 to 150/75 mg of cefotaxime/sulbactam per kg b.w. per day in three divided doses.
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Mitomycin Injection

Mitomycin Injection
  • Mitomycin Injection
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Product Details:

Type of MedicinesAllopathic
Dosage FormInjection
Grade standardMedicine Grade

  • Under the meticulous supervision of our highly professionals, we are providing high quality range of Mitomycin Injection to our clients.
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N-Acetyl Cysteine Injection

N-Acetyl Cysteine Injection
  • N-Acetyl Cysteine Injection
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Composition :400mg/2ml,1000mg/5ml
Indications :As a mucolytic in respiratory disorder associated with the production of viscous mucus such as acute and chronic bronchitis. In alveolar protenosis to remove proteinaceous material by repeated lavage with heparin and acetylcysteine which may prolong survival up to 5 years.
Dosage :Nebulisation : (Face mask, mouth piece, tracheostomy) 3-5ml of a 20% solution 3-4 times daily.
Orally : 200mg three times daily. Children up to 2 years may be given 200mg once daily and those between 2-6 years 200mg twice daily.
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Vincristine Injection

Vincristine Injection
  • Vincristine Injection
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Product Details:

TypeAllopathic
Form of MedicineInjection
UsageCommercial

Composition 1mg/ml,2mg/2ml
Indications Acute leukemia, lymphomas, Hodgkin's disease, non-Hodgkin lymphosarcoma, neuroblastoma, rhabdomyosarcoma, Wilm's tumour.
Contraindications Pregnancy, lactation, demyelinating form of Charcot Marie tooth disease.
Safety Profile The needle should be properly placed in the vein. If leakage occurs in surrounding tissues, considerable irritation will occur. Local injection of & moderate heat will minimize the discomfort. Used only by iv route. Considerable irritation can occur if extravasated into surrounding tissues.
Adverse Effects Hair loss, leucopenia, neuritic pain, constipation, sensory loss, paraesthesia, difficulty in walking, loss of deep tendon reflexes, muscle wasting, fever, hypersensitivity reaction, weight loss, polyuria, urinary retention, hypertension, cranial nerve palsies, headache, bone pains, parotid pain, myalgia, convulsions, syndrome of inappropriate secretion of ADH.
Drug Interactions If given with phenytoin, there is increased seizure activity. Acute bronchospasm with mitomycin-C.
Dosage Given iv at weekly intervals.
Children 2mg/m (if <10kg, start with 0.05mg/kg/week).
Adult 1.4 mg/m.
Decrease the dose to 50%, if S. bilirubin is >3mg/dl. Not given to patient getting radiation thereby through ports that include liver.
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Tobramycin Injection

Tobramycin Injection
  • Tobramycin Injection
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Product Details:

Dosage FormInjection

  • Category: Aminoglycosides
  • Each vial contains:- Tobramycin - 20mg, 60mg and 80mg
  • Quality Specification:-Chromatographic Purity - NLT 99.5%
Composition : 20mg/2 ml, 60mg/1.5ml, 80mg/2ml
TOBRAMYCIN: :-It is an aminoglycoside, highly soluble in water & stable for several week in solutions of various pH.
Indications :Treatment of external infection of the eye and its adnexa caused by susceptible strains of gram-positive, gram-negative & other probable bacteria. Safe & effective in children.
Dosage :-1-2 drops in the affected eye(s) every 4 hrs.
Adult :-Pneumonias, UTI, skin and skin structure infections: 500 mg 8 hourly.
Nosocomial Pneumonias, peritonitis, septicemia: 1gm every 8 hours.
Contra-Indications :-Hypersensitivity
Special Precautions :Not for injection into eye. If sensitivity reaction occurs, discontinue.
Paediatrics :-Safety is not established in patient with neutropenia or primary/secondary immuno-deficiency. Safety is not established in infants under 3 months of age.
Pregnancy :-Safety is not established.
Lactation :-Safety is not established.
Elderly :-Safe for elderly with normal renal functions.
Side-effects :-Localised ocular toxicity and hypersensitivity including itching and swelling and conjuctival erythema
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Dactinomycin Injection

Dactinomycin Injection
  • Dactinomycin Injection
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Product Details:

Form of MedicineInjection
UsageCommercial

  • Category Anti-neoplastic. Each vial contains Dactinomycin USP 500 mcg. Good evidence exists that this drug bind strongly, but reversibly, to DNA, interfering with synthesis of RNA (prevention of RNA polymerase elongation) and, consequently, with protein synthesis.
Specification-pH range- 5.5 to 7.5
Dactinomycin is a clear, gold-colored liquid given into a vein (IV).
A compound composed of a two cyclic peptides attached to a phenoxazine that is derived from streptomyces parvullus. It binds to DNA and inhibits RNA synthesis (transcription), with chain elongation more sensitive than initiation, termination, or release. As a result of impaired mRNA production, protein synthesis also declines after dactinomycin therapy.
Indication For treatment of Wilms' tumor, childhood rhabdomyosarcoma, Ewing's sarcoma and metastatic, nonseminomatous testicular cancer as part of a combination chemotherapy and/or multi-modality treatment regimen.
Dosage -Dose intensity per 2-week cycle for adults or children should not exceed 15 mcg/kg/day or 400-600 mcg/m/day intravenously for five days.
Contra Indications-Active infection with chiken pox or herpes zoster (a severe generalized form of disease may occure), infants less than12 months.
Precautions-This drug is not recommended for use during pregnancy. Precaution is advised when using this drug in the elderly because they may be more sensitive to the effects of the drug, especially the effect on blood cell production (myelosuppression).
Drug interaction Trastuzumab may increase the risk of neutropenia and anemia. Monitor closely for signs and symptoms of adverse events.
Adverse effects Nausea, vomiting, malaise, fatigue, cheilitis, dysphagia, bone marrow depression gastric ulceration, hepatitis, hepatomegaly, abnormal liver function, alopecia, skin eruotion.
StoragePowder for injection at room temperature (59 Degree to 86 DegreeF). Protect from light and humidity.
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Mitomycin Injection

Mitomycin Injection
  • Mitomycin Injection
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Product Details:

Product TypeFinished Product
Form of MedicineInjection
UsageCommercial

  • It is an antibiotic isolated from streptomyces caespitosis, It selectively inhibits synthesis of DNA.
Composition 2mg, 10mg & 40mg
Indications Disseminated adenocarcinoma of stomach and pancreas.
Contraindications Patients with previous idiosyncratic reaction to the drug, patient with thrombocytopenia, coagulation disorders, increase in bleeding tendency, pregnancy etc.
Adverse Effects Fever, anorexia, nausea, vomiting, bone marrow, depression (within 8 weeks of onset of therapy) etc. Cellulitis at injection site, stomatitis, alopecia, renal impairment, pulmonary toxicity, haemolytic uraemia syndrome (micro angiopathic haemolytic anaemia, thrombocytopenia, irreversible, renal failure), congestive heart failure, headache, visual blurring, diarrhoea, pain etc.
Drug Interactions Potentiates adriamycin induced cardiotoxicity. Synergestic with 5-flurouracil.
Dosage 20 mg/m i.v. single dose via 1/2 catheter. Patient should be fully evaluated after each course and dose decrease if toxicity appears.
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Octeriotide Injection

Octeriotide Injection
  • Octeriotide Injection
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Product Details:

Product TypeFinished Product
Medicine TypeAllopathic
UsageCommercial

  • Category: Liquid Ampoules / Vials
  • Each vial contains:-Octreotide 50 mcg & 100 mcg per ml
  • Quality Specification:-Chromatographic Purity: NLT 99.5%.

  • It is a analogue of somatostatin and is a growth inhibitor. It suppress the secretion the secretion of GH It have antisecretory action by inhibiting secretion of gastrin & secretin.
Composition : 50mcg/ml, 100mcg/ml
Indication :Insulinomas, zollinger Ellison syndrome, acromegaly, vasoactive intestinal peptide tumours.
Contraindications :-Hypersensitivity.
Safety Profile :-In pregnancy or nursing mothers, it may be used if potential benefits overcome potential risks.
Adverse Effects :-Anorexia, GIT upsets, bloating, pain at inj. Site, pancreatitis.
Drug Interactions :Cimetidine, cyclosporine, cyanocobalamin, insulin.
Dosage :-Initially 0.05 to 0.1mg S.C. every 8-12 hrs max. 1.5 mg daily.
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Cefoperazone Injection

Cefoperazone Injection
  • Cefoperazone Injection
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Product Details:

Product TypeFinished Product
Medicine TypeAllopathic
UsageCommercial

  • The drug will be either injected into a large muscle (such as your buttock or hip) or added to an intravenous fluid that will drip through a needle or catheter placed in your vein for 30 minutes, two to four times a day. Cefoperazone eliminates bacteria that cause many kinds of infections, including lung, skin, bone, joint, stomach, blood, gynecological, and urinary tract infections. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information. Your health care provider (doctor, nurse or pharmacist) may measure the effectiveness and side effects of your treatment using laboratory tests and physical examinations. It is important to keep all appointments with your doctor and the laboratory. The length of treatment depends on how your infection and symptoms respond to the medication.

Precautions Before administering cefoperazone

  • Tell your doctor and pharmacist if you are allergic to cefoperazone or any other cephalosporin [Cefaclor (Ceclor), Cefadroxil (Duricef) or Cephalexin (Keflex)], Penicillins or any other drugs.
  • Tell your doctor and pharmacist what prescription and nonprescription medications you are taking, especially other antibiotics, probenecid (Benemid) and vitamins.
  • Tell your doctor if you have or have ever had kidney, liver, gallbladder or gastrointestinal disease (Especially colitis).
Composition : 250mg,500mg,1gm,2 gm
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Methyl Prednisolone Succinate Injection

Methyl Prednisolone Succinate Injection
  • Methyl Prednisolone Succinate Injection
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Product Details:

Product TypeFinished Product
Medicine TypeAllopathic
UsageCommercial

  • Category: Antimalarial
Composition : 60mg
Artesunate: Artemisinin derivatives are the potent and rapidly acting blood schizonticides. These are cconcentrated in parasitized erythrocytes. Artesunate acts rapidly, stopping parasite development and preventing subsequent cytoadherence and resetting.Artesunate is well distributed and achieves high concentration in the intestines, liver and kidneys. Only a small amount of artesunate is excreted in the urine and in the stools.
Indications:Severe malaria including cerebral malaria and as a second line treatment in chloroquineresistant falciparum malaria.
Dosage : Adults : Parenteral:120gm on the first day followed by 60mg can be given on the first day itself 6 hours after the first dose.
Oral:100mg twice a day on the first day followed by 50mg twice daily for the next four days.
Children:1.2mg/kg x 5 days (maximum 60mg)
Contraindications: Not known
Special Precaution:Avoid in pregnant woman, especially in the first trimester.
Paediatrics:May be used if chloroquine resistant.
Pregnancy:Cpmtraomdocated on 1st trimester.
Lactation: Safety not established.
Side-Effects: Transient and reversible reticulocytopenia, drug fever, drug rash, bradycardia, transient first degree heart block and transient & revesible elevation of serum transaminases.
Lactation: Safety not established.
Drug Interactions: Antimalarial action potentiated by oxidant drugs. Additive effect seen with chloroquine. Antagonistic effect seen with pyrinethamine and sulfonamides.
Purity :Not less than 99%.
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Dopamine Injection

Dopamine Injection
  • Dopamine Injection
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Product Details:

Product TypeFinished Product
Medicine TypeAllopathic
Usage/ApplicationCommercial

Dopamine injection is used to treat certain conditions that occur when you are in shock, which may be caused by heart attack, trauma, surgery, heart failure, kidney failure, and other serious medical conditions.
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Irinotecan Injection

Irinotecan Injection
  • Irinotecan Injection
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Product Details:

TypeAllopathic
Form of MedicineInjection

  • 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.
.
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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Topotecan Injection

Topotecan Injection
  • Topotecan Injection
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Product Details:

TypeAllopathic
Form of MedicineInjection
UsageCommercial

  • 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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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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Leuprolide Injection

Leuprolide Injection
  • Leuprolide Injection
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Product Details:

TypeAllopathic
UsageCommercial
Form of MedicineInjection

  • 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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Dacarbazine Injection

Dacarbazine Injection
  • Dacarbazine Injection
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Product Details:

Form of MedicineInjection
UsageCommercial

  • Category: Anti-neoplastic. Each lyophilized vial contains:- Dacarbazine USP 100mg/ 200 mg/ 500mg 
It is an unidarole derivative. Exact mechanism 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. Hodgkin's disease : 150mg/m² to be repeated every 15 days.
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. Effect decreased by CYP1A2 inducers e.g. aminoglutethimide, carbamazepine, phenobarbital 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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Daunorubicin Injection

Daunorubicin Injection
  • Daunorubicin Injection
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Product Details:

Product TypeFinished Product
Form of MedicineInjection
UsageCommercial

  • 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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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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Fludarabine Injection

Fludarabine Injection
  • Fludarabine Injection
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Product Details:

FormInjection

  • 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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Analgin Injection

Analgin Injection
  • Analgin Injection
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Product Details:

Product TypeFinished Product
Medicine TypeAllopathic
Usage/ApplicationCommercial

  • 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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Fludarabine Injection

Fludarabine Injection
  • Fludarabine Injection
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Product TypeFinished Product
Usage/ApplicationCommercial

  • 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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Alpha Beta Arteether Injection

Alpha Beta Arteether Injection
  • Alpha Beta Arteether Injection
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Product Details:

Dosage FormInjection

  • 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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Artemether Injection

Artemether Injection
  • Artemether Injection
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Product TypeFinished Product
Medicine TypeAllopathic
Usage/ApplicationCommercial

  • 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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Adenosine Injection

Adenosine Injection
  • Adenosine Injection
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Product TypeFinished Product
Usage/ApplicationCommercial

  • 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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Bleomycin Injection

Bleomycin Injection
  • Bleomycin Injection
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Product Details:

TypeAllopathic
Form of MedicineInjection
UsageCommercial

  • 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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Esomeprazole Injection

Esomeprazole Injection
  • Esomeprazole Injection
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Product Details:

Dosage FormInjection

Esomeprazole Injection is a proton pump inhibitor used in the treatment of stomach ulcers, Gastroesophageal reflux disease(GERD) and other acidity related disorders. It decreases the acid produced in the stomach and also helps in the healing of ulcers.

Esomeprazole 40mg Injection
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Heparin Injection

Heparin Injection
  • Heparin Injection
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Product TypeFinished Product
UsageCommercial, Clinical, Hospital

This medication is used to prevent and treat blood clots. It may be used to treat blood clots in the lungs/legs. It may also be used to prevent blood clots after surgery, during dialysis, when collecting blood samples, or when a person is unable to move for a long time. Heparin helps to keep blood flowing smoothly by making a certain natural substance in your body (anti-clotting protein) work better. It is known as an anticoagulant.

How to use
: This medication is given by injection by a health care professional. Learn all preparation and usage instructions for this product. Before using this product, check it visually for particles or discoloration. If either is present, do not use the liquid. If you have questions about the use of this medication, consult the doctor or pharmacist. Do not inject this medication into a muscle. For products given under the skin, clean the injection site with rubbing alcohol before injecting each dose. It is important to change the location of the injection site daily to avoid problem areas under the skin.

Side effects:
Mild pain/redness/irritation at the injection site may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly. This medication can cause bleeding if it has too much effect on your blood. Tell your doctor immediately if you develop any signs of serious bleeding, including unusual pain/swelling/discomfort, prolonged bleeding from cuts or gums, persistent nosebleeds, unusually heavy/prolonged menstrual periods, unusual/easy bruising, dark urine, black stools, severe headache, unusual dizziness. (See also Precautions section regarding HIT). Tell your doctor immediately if any of these unlikely but serious side effects occur: swelling at injection site, bone pain, easily broken bones. Seek immediate medical attention if any of these rare but very serious side effects occur (see also Precautions section regarding HIT): pain/loss of feeling in the arms/legs, change in color of the arms/legs, chest pain, trouble breathing, confusion, weakness on one side of the body, slurred speech, vision changes. A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any symptoms of a serious allergic reaction, including: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing.
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Human Menopausal Gonadotrophins (HMG) Injections

Human Menopausal Gonadotrophins (HMG) Injections
  • Human Menopausal Gonadotrophins (HMG) Injections
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Prescription/Non prescriptionPrescription
Usage/ApplicationCommercial
Medicine TypeInjection

Human menopausal gonadotropin, which is the primary constituent of Hmg Sp 75 IU Injection, is obtained from the urine of women who have achieved menopause. It is used to treat male and female infertility. It is also used in combination with other hormonal medicines for in vitro fertilization and assisted reproduction procedures.
Human Menopausal Gonadotrophins (HMG) 75IU/150IU Injections
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Noradrenaline Injection

Noradrenaline Injection
  • Noradrenaline Injection
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Product Details:

UsageHospital
Product TypeFinished Product
Usage/ApplicationCommercial

Noradrenaline Injection is the generic form of the brand-name prescription drug Levophed, used to treat life-threatening conditions such as shock and low blood pressure (also known as hypotension).
Noradrenaline 4mg/2ml Injection
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Doripenem Injection

Doripenem Injection
  • Doripenem Injection
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Product TypeFinished Product
Usage/ApplicationCommercial

Doripenem injection is used to treat serious infections of the urinary tract, kidney, and abdomen that are caused by bacteria. Doripenem injection is not approved by the Food and Drug Administration (FDA) to treat pneumonia that developed in people who were on a ventilator in a hospital. Doripenem injection is in a class of medications called carbapenem antibiotics. It works by killing bacteria.
Doripenem 500mg Injection
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Imipenem Cilastatin Injection

Imipenem Cilastatin Injection
  • Imipenem Cilastatin Injection
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Product TypeFinished Product
Injectable FormInjection
Usage/ApplicationCommercial

Imipenem and cilastatin injection is used to treat certain serious infections that are caused by bacteria, including endocarditis (infection of the heart lining and valves) and respiratory tract (including pneumonia), urinary tract, abdominal (stomach area), gynecological, blood, skin, bone, and joint infections. Imipenem is in a class of medications called carbapenem antibiotics. It works by killing bacteria. Cilastatin is in a class of medications called dehydropeptidase inhibitors. It works by helping imipenem stay active in your body for a longer period of time.


Imipenem 250mg + Cilastatin 250mg Injection
Imipenem 500mg + Cilastatin 500mg Injection
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Meropenem Sulbactam Injection

Meropenem Sulbactam Injection
  • Meropenem Sulbactam Injection
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Product Details:

Injectable FormInjection
Medicine TypeAllopathic

Meropenem / Sulbactam is used for Bacterial infections, Lung infections, Bronchial infections, Infections during delivery, Infections after delivery, Management of reduced white blood cells patients with fever, Bacterial blood poisoning, Intraabdominal infections, Gynecological infections, Skin or soft tissue infections and other conditions.

 

Meropenem Sulbactam 1.5gm Injection

 

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