FDA NDC Directory · JSON-LD · Markdown

Floxuridine

NDC 63323-145 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameFLOXURIDINE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075837
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRA-ARTERIAL
Active ingredientsFLOXURIDINE (500 mg/5mL)
Marketing started20010315
Package count1

External sources

Source: openFDA. Public-domain (CC0).