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Gemcitabine

NDC 25021-239 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namegemcitabine
Labeler / ManufacturerSagent Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA209077
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsGEMCITABINE HYDROCHLORIDE (38 mg/mL)
Marketing started20190115
Package count3

External sources

Source: openFDA. Public-domain (CC0).