FDA NDC Directory · JSON-LD · Markdown

gemcitabine hydrochloride

NDC 68083-149 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA204520
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsGEMCITABINE HYDROCHLORIDE (1 g/25mL)
Marketing started20160201
Package count1

External sources

Source: openFDA. Public-domain (CC0).