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Ceftriaxone Sodium

NDC 0409-7336 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerHospira, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA065204
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsCEFTRIAXONE SODIUM (2 g/1)
Marketing started20050720
Marketing ended20270430
Package count1

External sources

Source: openFDA. Public-domain (CC0).