FDA NDC Directory · JSON-LD · Markdown

GEMCITABINE

NDC 63323-125 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090799
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsGEMCITABINE HYDROCHLORIDE (1 g/25mL)
Marketing started20110726
Package count1

External sources

Source: openFDA. Public-domain (CC0).