Product Description
Since last manyyears SaintroyLifescienceis leading manufacture, export and supplierofIrinotecan Hydrochloride Injectionfrom Surat, Gujarat, India. Irinotecan Hydrochloride Injection used to treat colon cancer, and small cell lung cancer.For colon cancer it is used either alone or with fluorouracil.
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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 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 Lifescience Irinotecan HydrochlorideInjection export 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,Hong Kong, 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 in Oncology TreatmentIrinotecan Hydrochloride Injection is designed for hospital and clinical use through intravenous infusion. Suitable for dealer, distributor, exporter, manufacturer, supplier, trader, and wholesaler needs in India, this product ensures consistent quality and compliance. The solution is effective in inhibiting DNA topoisomerase I, targeting cancer cell replication in colorectal and other solid tumors.
Trusted Standards and ComplianceThis injection meets rigorous USP standards and is manufactured in ISO 9001-certified, WHO-GMP-approved facilities. Each glass vial is sterile, nonpyrogenic, and tailored for professional healthcare administration after proper dilution. The packaging choices provide flexibility for diverse patient and clinical requirements.
FAQ's of Irinotecan Hydrochloride Injection:
Q: How should Irinotecan Hydrochloride Injection be prepared and administered?
A: Irinotecan Hydrochloride Injection must be diluted according to the specific prescribing information before intravenous infusion. Administration should only occur under the supervision of medical professionals who are experienced in chemotherapy.
Q: What is the primary indication for using Irinotecan Hydrochloride Injection?
A: This injection is primarily indicated for the treatment of metastatic colorectal cancer and may also be used for other solid tumors as determined by an oncologist.
Q: When is Irinotecan Hydrochloride Injection contraindicated?
A: The injection is contraindicated in patients with known hypersensitivity to Irinotecan or any of its excipients. Always review patient history before use.
Q: Where should Irinotecan Hydrochloride Injection be stored?
A: The product should be stored in a cool and dry place, away from direct sunlight, to maintain its stability and efficacy throughout its two-year shelf life.
Q: What is the benefit of Irinotecan Hydrochloride Injection in cancer therapy?
A: Irinotecan Hydrochloride acts by inhibiting DNA topoisomerase I, interfering with the replication of cancer cells, which can help slow tumor growth and support treatment outcomes.
Q: What should be done if the solution in the vial appears discolored or cloudy?
A: Only use vials containing a clear, pale yellow solution. Do not use if the solution appears cloudy, discolored, or contains particles; such vials should be discarded according to safety protocols.
Q: Is the fermentation smell in Irinotecan Hydrochloride Injection normal?
A: Yes, a mild fermentation-like smell is considered normal and does not indicate a problem with the product's quality or usability.