FDA NDC Directory · JSON-LD · Markdown

Cefoxitin

NDC 25021-110 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Generic namecefoxitin
Labeler / ManufacturerSagent Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA065414
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsCEFOXITIN SODIUM (2 g/1)
Marketing started20091105
Package count1

External sources

Source: openFDA. Public-domain (CC0).