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Cefazolin

NDC 0143-9665 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065143
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsCEFAZOLIN SODIUM (20 g/1)
Marketing started20041018
Package count1

External sources

Source: openFDA. Public-domain (CC0).