L-ASPARIGENASE INJECTION 10000 IU

100 INR/Unit

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Product Details:

Dosage Form Injection
Salt Composition L-Asparaginase 10,000 IU per vial
Indication Acute lymphoblastic leukemia, lymphosarcoma, malignant diseases
Enzyme Types L-Asparaginase enzyme (EC 3.5.1.1)
Feature High purity, sterile, pyrogen-free, clinical grade
Ingredients L-Asparaginase, excipients, lyophilized powder
Application Parenteral (intravenous or intramuscular) administration in oncology
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L-ASPARIGENASE INJECTION 10000 IU Price And Quantity

Minimum Order Quantity 1000 , , Unit
Price 100 INR/Unit

L-ASPARIGENASE INJECTION 10000 IU Product Specifications

Enzyme Types L-Asparaginase enzyme (EC 3.5.1.1)
Enzymatic Activity 10,000 IU/vial on reconstitution
Dosage Form Injection
Ph Level 7.0-7.5 (buffered during preparation)
Feature High purity, sterile, pyrogen-free, clinical grade
Salt Composition L-Asparaginase 10,000 IU per vial
Fermentation Smell Odorless or faint fermentation odor
Storage Instructions AS PER INSTRUCTIONS
Application Parenteral (intravenous or intramuscular) administration in oncology
Indication Acute lymphoblastic leukemia, lymphosarcoma, malignant diseases
Physical Color/Texture White to off-white, lyophilized powder
Ingredients L-Asparaginase, excipients, lyophilized powder

Solubility Soluble after reconstitution with provided diluent
Pack Size 1 vial per carton, may include sterile diluent
Reconstitution Volume To be reconstituted with sterile water for injection as per physician's instructions
Preparation Time Should be used immediately after reconstitution
Contraindications Hypersensitivity to L-asparaginase or its components
Compatibility Compatible with standard IV fluids when administered as per guidelines
Adverse Effects Hypersensitivity reactions, pancreatitis, coagulopathy, hepatotoxicity
Caution Monitor for allergic or hypersensitivity reactions during administration
Market Approval Approved by relevant regulatory authorities for therapeutic use
Dispensing To be used by qualified healthcare professionals only
Sterility Sterile lyophilized powder for injection
Route of Administration IV (intravenous) or IM (intramuscular)
Preservative Free Yes
Microbial Source Produced by fermentation using genetically derived E. coli or Erwinia chrysanthemi

L-ASPARIGENASE INJECTION 10000 IU Trade Information

FOB Port AHEMDABAD, MUNDRA & MUMBAI
Supply Ability 10000 , , Unit Per Month
Delivery Time 4 Week
Sample Available Yes
Sample Policy Free samples available with shipping and taxes paid by the buyer
Packaging Details AS PER REQUIREMENT
Main Domestic Market All India
Certifications WHO-GMP

Product Description

PRODUCT NAME: L-ASPARIGENASE INJECTION 10000 IU

PACKING: FOR SINGLE VIAL

COMPANY: OCEAN PHARMACEUTICAL

USES: L-ASPARIGENASE INJECTION 10000 IU Injection is used in the treatment of some kinds of cancer of white blood cells (leukemia). It may also be used to treat other types of cancer as determined by your doctor. It may be used on its own, or sometimes given together with certain other medicines as part of combination chemotherapy.

About the Product

L-ASPARAGINASE INJECTION 10,000 IU is produced by fermentation from recombinant E. coli or Erwinia chrysanthemi, ensuring a high-purity, clinical grade preparation. Featuring a buffered pH of 7.0-7.5, it presents as a white to off-white lyophilized powder, specifically indicated for oncology applications. Each vial delivers 10,000 IU of active enzyme, guaranteeing reliable enzymatic activity upon reconstitution.

Usage & Administration

Designed for parenteral use, this injection can be administered either intravenously or intramuscularly under a physician's supervision. Reconstitution involves mixing with sterile water as directed by a healthcare provider, enabling immediate solubility and use. Monitoring for allergic or hypersensitivity reactions during administration is crucial due to potential adverse effects.

Quality & Safety

Manufactured to ensure sterility and the absence of preservatives, this injection meets stringent regulatory approvals for therapeutic use in oncology. Only qualified healthcare professionals should dispense and administer the product, ensuring patient safety and optimal treatment efficacy. Regular guidance for storage and handling must be followed to maintain its pharmaceutical integrity.

FAQ's of L-ASPARIGENASE INJECTION 10000 IU:

Q: How is L-ASPARAGINASE INJECTION 10,000 IU prepared for administration?

A: The injection should be reconstituted with sterile water for injection, using the volume recommended by the physician. After addition of the diluent, gently swirl the vial until the lyophilized powder is fully dissolved, ensuring the solution is clear before administration.

Q: What is the appropriate route of administration for this medication?

A: L-ASPARAGINASE INJECTION can be given either intravenously (IV) or intramuscularly (IM), depending on the treatment protocol and the patient's clinical condition as decided by the healthcare provider.

Q: When should the reconstituted solution be used?

A: After reconstitution, the solution should be used immediately to preserve enzymatic activity and prevent contamination. Discard any leftover solution as per safety guidelines.

Q: Where should the L-ASPARAGINASE INJECTION be stored before use?

A: Store the unopened vial as per the instructions provided on the package insert, usually at controlled room temperature or refrigerated, away from light and moisture. Consult the physician or pharmacist for specific storage recommendations.

Q: What process ensures the sterility and quality of this injection?

A: The product is manufactured under strict sterile conditions using lyophilization, with comprehensive quality controls to confirm its pyrogen-free and high-purity status. Regulatory bodies have approved it for safe therapeutic use.

Q: What are the benefits of using L-ASPARAGINASE INJECTION in oncology?

A: It effectively targets malignant cells by depleting asparagine, which certain cancer cells need to survive, thereby aiding in the treatment of acute lymphoblastic leukemia and related malignancies. This targeted mechanism can improve outcomes in eligible patients.

Q: What precautions are necessary during its administration?

A: During administration, close monitoring for signs of hypersensitivity or allergic reactions is essential. The product should be dispensed and administered only by qualified medical professionals according to established oncology protocols.

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