FDA NDC Directory · JSON-LD · Markdown

Gemcitabine

NDC 0409-0181 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameGEMCITABINE
Labeler / ManufacturerHospira, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA200795
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsGEMCITABINE HYDROCHLORIDE (38 mg/mL)
Marketing started20110826
Package count1

External sources

Source: openFDA. Public-domain (CC0).