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Ceftriaxone Sodium

NDC 67184-1007 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerQilu Pharmaceutical Co., Ltd.
Marketing categoryAbbreviated NDA (generic) · App ANDA203702
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsCEFTRIAXONE SODIUM (1 g/1)
Marketing started20160629
Package count1

External sources

Source: openFDA. Public-domain (CC0).