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Ceftriaxone Sodium

NDC 76420-596 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203702
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsCEFTRIAXONE SODIUM (500 mg/1)
Marketing started20170630
Package count2

External sources

Source: openFDA. Public-domain (CC0).