FDA NDC Directory · JSON-LD · Markdown

CEFAZOLIN

NDC 63323-236 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Generic nameCEFAZOLIN SODIUM
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA065303
Dosage form / routePOWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsCEFAZOLIN SODIUM (500 mg/2.2mL)
Marketing started20110715
Package count1

External sources

Source: openFDA. Public-domain (CC0).