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Ceftriaxone Sodium

NDC 71205-710 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA065169
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsCEFTRIAXONE SODIUM (2 g/1)
Marketing started20050509
Package count1

External sources

Source: openFDA. Public-domain (CC0).