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GEMCITABINE

NDC 0409-0187 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerHospira, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079183
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsGEMCITABINE HYDROCHLORIDE (38 mg/mL)
Marketing started20101115
Package count1

External sources

Source: openFDA. Public-domain (CC0).