Product Description
Since last manyyears Saintroy Lifescience is leading manufacture, export and supplierofL-Asparaginase Injection from Surat, Gujarat, India. L-Asparaginase Injectionused as a medication and in food manufacturing.
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ISO/GMP/cGMP/WHOGMP/NAFDAC approved, PPB Kenya approved/USFDA approved/EUGMP approved/MOH Iran approved manufacturingfacility in Gujarat, India.
Registration: Saintroy Lifescience is interested in registrationof own brand or customer brands in ministry of health of clientscountry and we also provide the products samples, COA, COPP, ACTD or CTD dossier, DMF, Manufacturing license, Free sales certificate and other required documents.
Export Country :Saintroy Lifescience L-Asparaginase Injectionexport to USA, Canada, Germany, Europe, France, Ghana, Nigeria,Kenya, Senegal, Sudan,UAE, Kuwait, Dubai, Cameroon, Lebanon, Peru, Chile,Somalia, Philippines, Myanmar, Maldives, Thailand, Singapore, Malaysia, HongKong, China, Zimbabwe, Togo, Burkina Faso, Niger,Guinea Bissau, Congo,Democratic of republic, Ivory Costa, Oman, Guatemala, Nicaragua, Salvador,Qatar, Costa Rica, Panama, Cuba, Colombia, Bolivia, Argentine, Algeria, Guyana,Morocco, Jordan, Bahrain, Iran, Egypt, Kyrgyzstan, Uzbekistan, Kazakhstan.
Precise Therapeutic ActionL-Asparaginase Injection disrupts the synthesis of asparagine, effectively inhibiting cancer cell growth in patients diagnosed with Acute Lymphoblastic Leukemia (ALL). Its mode of action targets rapidly dividing cells, providing an essential tool in multi-agent chemotherapy regimens.
Strict Quality and Safety ComplianceProduced in adherence with GMP and WHO guidelines, each batch of L-Asparaginase Injection is rigorously tested to ensure microbial purity and consistent enzymatic activity. The product is packaged in USP Type I glass vials, ensuring maximum stability and patient safety.
Flexible Administration and StorageThe injection can be administered either intramuscularly or intravenously after reconstituting with sterile water. It should be stored in a cool, dry place and has a limited shelf life of 2 days post-reconstitution, supporting optimal enzyme efficacy during use.
FAQ's of L-Asparaginase Injection:
Q: How should L-Asparaginase Injection be prepared and administered?
A: L-Asparaginase Injection should be reconstituted with sterile water for injection according to the vial instructions. Once dissolved, it can be administered either intramuscularly or intravenously by qualified medical professionals.
Q: What is the main benefit of using L-Asparaginase Injection in treatment?
A: The principal benefit of L-Asparaginase Injection is its ability to target and reduce asparagine levels, thereby inhibiting the proliferation of leukemic cells in Acute Lymphoblastic Leukemia (ALL) patients.
Q: When should this injection be avoided?
A: L-Asparaginase Injection should not be used in individuals with known hypersensitivity to L-Asparaginase or any of its ingredients, as severe allergic reactions may occur.
Q: What is the shelf life of the reconstituted injection, and how should it be stored?
A: After reconstitution, the injection must be used within 2 days and stored in a cool, dry place to maintain efficacy and prevent contamination.
Q: Where is this product manufactured and to what standards?
A: It is manufactured in India under strict Good Manufacturing Practices (GMP) and World Health Organization (WHO) guidelines, ensuring quality and safety for medical use.
Q: What are the physical characteristics of the product and its solution?
A: The product is a white to off-white lyophilized powder, which, upon reconstitution with sterile water, results in a clear solution with a pH of 6.5 to 7.5 and is free from bacterial endotoxins.