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Gemcitabine

NDC 0409-0185 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameGEMCITABINE
Labeler / ManufacturerHospira, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078339
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsGEMCITABINE HYDROCHLORIDE (38 mg/mL)
Marketing started20110726
Package count1

External sources

Source: openFDA. Public-domain (CC0).