FDA NDC Directory · JSON-LD · Markdown

Cefazolin

NDC 63323-238 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Generic nameCefazolin Sodium
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA065306
Dosage form / routePOWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsCEFAZOLIN SODIUM (10 g/1)
Marketing started20110614
Package count1

External sources

Source: openFDA. Public-domain (CC0).