L-Asparaginase Injection

1 USD ($)/Box

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Product Details:

Dosage Form Injection
Salt Composition L-Asparaginase
Indication Acute lymphoblastic leukemia (ALL), lymphoblastic lymphoma
Enzyme Types Other
Feature Other
Ingredients Other
Application Other
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L-Asparaginase Injection Price And Quantity

Price 1 USD ($)/Box
Minimum Order Quantity 100 Box

L-Asparaginase Injection Product Specifications

Ingredients Other
Application Other
Storage Instructions Store at cool and dry place.
Physical Color/Texture White to off-white, lyophilized powder or crystalline solid
Shelf Life 2 Years
Fermentation Smell Normal Smell
Ph Level 6.5 - 7.5
Temperature Needed For Fermentation 30C - 37C
Enzyme Types Other
Dosage Form Injection
Enzymatic Activity Minimum 10,000 IU/vial (varies by brand and strength)
Feature Other
Indication Acute lymphoblastic leukemia (ALL), lymphoblastic lymphoma
Salt Composition L-Asparaginase

Contraindication Known hypersensitivity to L-Asparaginase or its components
Allergenicity Potential for hypersensitivity or allergic reactions
Manufacturing Standard Manufactured under GMP/WHO-GMP certified facility
Purity >98% (HPLC analysis standard)
Preservative Preservative-free
Mode of Administration Intravenous or intramuscular as per medical advice
Microbial Limit Complies with pharmacopeial standards
Packaging Size Available in single-use vials (e.g., 10,000 IU, 5,000 IU, or as specified)
Reconstitution Requirement To be reconstituted with sterile water for injection

L-Asparaginase Injection Trade Information

FOB Port surat
Payment Terms Cash on Delivery (COD), Letter of Credit (L/C), Paypal, Delivery Point (DP), Western Union, Letter of Credit at Sight (Sight L/C), Cash Against Delivery (CAD), Telegraphic Transfer (T/T), Days after Acceptance (DA), Cash in Advance (CID), Cheque, Cash Advance (CA)
Supply Ability 1000000 Box Per Month
Delivery Time 4 Days
Sample Policy Contact us for information regarding our sample policy
Packaging Details 1 Vial
Main Export Market(s) South America, Western Europe, Asia, Australia, North America, Eastern Europe, Middle East, Africa, Central America
Main Domestic Market Tripura, Manipur, Dadra and Nagar Haveli, Himachal Pradesh, Andaman and Nicobar Islands, Nagaland, Uttarakhand, Daman and Diu, Lakshadweep, South India, Central India, North India, East India, West India, Andhra Pradesh, Assam, Arunachal Pradesh, Bihar, Chandigarh, Delhi, Gujarat, Goa, Jammu and Kashmir, Jharkhand, Karnataka, Maharashtra, Mizoram, Meghalaya, Punjab, Pondicherry, Rajasthan, Sikkim, Tamil Nadu, Telangana, Uttar Pradesh, West Bengal, Haryana, Madhya Pradesh, Kerala, Odisha, Chhattisgarh, All India
Certifications ISO/GMP/c-GMP/WHOGMP/USFDA/EUGMP.

Product Description

Since last manyyears SaintroyLifescienceis leading manufacture, export and supplierofL-Asparaginase Injection from Surat, Gujarat, India. L-Asparaginase Injectionused as a medication and in food manufacturing.

Tags: L-Asparaginase Injection manufacturer, L-Asparaginase Injection exporter, L-Asparaginase Injection supplier,and L-Asparaginase Injection, whogmp approved L-Asparaginase Injection Manufacturerand supplier, L-Asparaginase Injection distributor, L-Asparaginase Injectionshipper, L-Asparaginase Injection 5000 I.UL-Asparaginase Injection 5000 I.Usupplier,L-Asparaginase Injection 5000 I.U.

ISO/GMP/cGMP/WHOGMP/NAFDAC approved, PPB Kenya approved/USFDA approved/EUGMP approved/MOH Iran approved manufacturingfacility in Gujarat, India.

Registration: Saintroy Lifescienceis interested in registrationof own brand or customer brands in ministryof 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 LifescienceL-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.

Precision Manufacturing and Purity

Produced under stringent GMP and WHO-GMP certified protocols, this L-Asparaginase Injection guarantees over 98% purity, ensuring reliable performance in clinical settings. Each vial undergoes thorough HPLC analysis and conforms to pharmacopeial microbial limits, making it suitable for critical oncology treatments.

Flexible Administration and Storage

L-Asparaginase Injection is supplied in single-use vials with strengths as specified (e.g., 10,000 IU, 5,000 IU). It must be reconstituted with sterile water for injection and is intended for hospital or clinic administration via intravenous or intramuscular injection. To maintain stability and efficacy, store vials in a cool, dry place.

FAQ's of L-Asparaginase Injection:

Q: How should L-Asparaginase Injection be prepared and administered?

A: The lyophilized powder must be reconstituted with sterile water for injection prior to use. Once prepared, it should be administered intravenously or intramuscularly, as directed by a healthcare professional.

Q: What conditions is L-Asparaginase Injection used to treat?

A: L-Asparaginase Injection is primarily indicated for the treatment of acute lymphoblastic leukemia (ALL) and lymphoblastic lymphoma in both pediatric and adult patients.

Q: When should L-Asparaginase Injection not be used?

A: This medication should not be used in individuals who have a known hypersensitivity to L-Asparaginase or any of its components, due to the risk of severe allergic reactions.

Q: Where should the reconstituted medication be stored?

A: Following reconstitution, it is recommended to use the injection immediately. Unused reconstituted solution should be discarded, while unopened vials must be stored in a cool and dry place as per storage guidelines.

Q: What is the process for ensuring the safety and quality of each vial?

A: Each vial of L-Asparaginase Injection is manufactured in a GMP/WHO-GMP certified facility, tested for purity (over 98% by HPLC), and complies with pharmacopeial microbial standards to guarantee patient safety.

Q: What are the benefits of choosing this preservative-free L-Asparaginase formulation?

A: This product's preservative-free nature reduces the risk of adverse reactions while providing consistent enzymatic activity. Its high purity and compliance with international manufacturing standards offer clinicians reliable and safe therapy options.

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