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Ceftriaxone Sodium

NDC 0409-7337 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerHospira, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA065169
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsCEFTRIAXONE SODIUM (250 mg/1)
Marketing started20050509
Package count1

External sources

Source: openFDA. Public-domain (CC0).