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Cefazolin

NDC 60505-6243 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA203661
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsCEFAZOLIN SODIUM (1 g/1)
Marketing started20220901
Package count1

External sources

Source: openFDA. Public-domain (CC0).