Cytotoxic Agent
Gemcitabine is a potent cytotoxic drug. Handle with extreme caution using appropriate personal protective equipment (PPE) including gloves, masks, and eye protection.
Eyes: Flush with water for 15 minutes and seek immediate medical attention.
Skin: Wash thoroughly with soap and water; remove contaminated clothing.
Gemcitabine (CAS 122111-03-9) is a deoxycytidine analog that functions as an antimetabolite, effectively inhibiting DNA synthesis in rapidly dividing cancer cells. In the pharmaceutical industry, it is widely utilized for the production of injectable formulations used in treating pancreatic, non-small cell lung, and ovarian cancers.
In the Indian market, Gemcitabine is a high-value specialty API manufactured by leading pharmaceutical companies for both domestic oncology portfolios and global exports. The Indian supply chain for this chemical is strictly regulated, requiring compliance with GMP (Good Manufacturing Practices) and stringent quality documentation for procurement.
Buyers should prioritize suppliers who provide comprehensive Certificate of Analysis (CoA), Drug Master File (DMF) support, and stability data. Given its sensitivity to environmental factors, procurement should focus on cold-chain logistics and verified pharmaceutical-grade packaging to ensure the integrity of the molecule during transit.
Gemcitabine pricing in India depends on grade, order quantity, and delivery location, and it moves with market conditions — so a single fixed price is rarely accurate for a specific requirement.
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Gemcitabine prices in India vary by grade, order quantity and delivery location, and move with market conditions. To get the current price for your requirement, submit an enquiry on Chemical Dekho and receive verified quotes from suppliers and manufacturers within 24 hours.
No, this is a prescription-only pharmaceutical API intended for licensed manufacturers and research institutions.
Every shipment includes a Certificate of Analysis (CoA), Material Safety Data Sheet (MSDS), and batch-specific quality reports.
Yes, to maintain stability and potency, it must be transported under controlled refrigerated conditions.
Yes, most Indian manufacturers provide DMF support for regulatory filings.
Lead times vary based on batch availability and regulatory documentation, typically ranging from 4 to 8 weeks.
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