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Gemcitabine

NDC 72485-222 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameGEMCITABINE HYDROCHLORIDE
Labeler / ManufacturerArmas Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210991
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsGEMCITABINE HYDROCHLORIDE (1 g/26.3mL)
Marketing started20200115
Package count1

External sources

Source: openFDA. Public-domain (CC0).