FDA NDC Directory · JSON-LD · Markdown

GEMCITABINE

NDC 68001-359 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryNew Drug Application (innovator) · App NDA209604
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsGEMCITABINE HYDROCHLORIDE (100 mg/mL)
Marketing started20180525
Package count1

External sources

Source: openFDA. Public-domain (CC0).