Product Description
Since last manyyears SaintroyLifescienceis leading manufacture, export and supplierofCytarabine Injectionfrom Surat, Gujarat, India. Cytarabine Injection used in the treatment of acute myeloid leukaemia, acute lymphocytic leukaemia (ALL) and in lymphomas.
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ISO/GMP/cGMP/WHOGMP/NAFDAC approved, PPB Kenya approved/USFDA approved/EUGMP approved/MOH Iran approved manufacturing facility inGujarat, India.
Registration: Saintroy Lifescienceis interested inregistration of 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 LifescienceCytarabine Injection Exportto USA, Canada, Germany, Europe, France, Ghana, Nigeria, Kenya, Senegal,Sudan,UAE, Kuwait, Dubai, Cameroon, Lebanon, Peru, Chile, Somalia, Philippines,Myanmar, Maldives, Thailand, Singapore, Malaysia, Hong Kong, China, Zimbabwe,Togo, Burkina Faso, Niger,Guinea Bissau, Congo, Democratic of republic, IvoryCosta, Oman, Guatemala, Nicaragua, Salvador, Qatar, Costa Rica, Panama, Cuba,Colombia, Bolivia, Argentine, Algeria, Guyana, Morocco, Jordan, Bahrain, Iran,Egypt, Kyrgyzstan, Uzbekistan, Kazakhstan.
Reliable Cancer TreatmentCytarabine Injection is a trusted medication for managing various hematological cancers, including AML, ALL, CML, and non-Hodgkin lymphoma. Its formulation allows flexibility in administration and integration into diverse chemotherapy protocols, supporting improved patient outcomes.
Quality and Safety ComplianceManufactured to rigorous USP/EP/BP standards, the injection ensures pharmaceutical quality and patient safety. The use of sterile glass vials and precise compounding techniques help maintain product efficacy and sterility throughout its shelf life.
User and Storage GuidelinesHealthcare professionals should administer Cytarabine Injection intravenously or subcutaneously, diluting with compatible IV fluids as required. Single-use vials should be discarded after opening. Store the vials in a cool, dry setting to preserve their integrity over the product's two-year shelf life.
FAQ's of Cytarabine Injection:
Q: How should Cytarabine Injection be prepared and administered?
A: Cytarabine Injection must be administered by a healthcare professional either intravenously or subcutaneously. It may be diluted with compatible IV fluids as recommended. Use only as a single-dose injection and discard any unused portion after use.
Q: What types of cancers is Cytarabine Injection prescribed for?
A: This injection is indicated for the treatment of certain cancers, specifically acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), chronic myeloid leukemia (CML), and non-Hodgkin lymphoma.
Q: Where and how should Cytarabine Injection be stored?
A: Keep the vials in a cool and dry place, following standard storage protocols for cytotoxic medications. Ensure they are kept away from direct sunlight and are not exposed to temperature extremes to maintain stability.
Q: When should the unused portion of a vial be discarded?
A: Each glass vial is intended for single use only. Any remaining solution after administration must be discarded immediately to prevent contamination and ensure patient safety.
Q: What are the key benefits of using Cytarabine Injection?
A: Cytarabine Injection provides effective treatment for various blood cancers, supports tailored chemotherapy regimens, and is manufactured to high quality standards ensuring reliable potency and patient safety.
Q: What is the physical appearance and pH of Cytarabine Injection?
A: The solution is clear, colorless, and has a neutral pH of approximately 7.0, making it suitable for safe administration without causing significant irritation.