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Famotidine

NDC 70860-751 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namefamotidine
Labeler / ManufacturerAthenex Pharmaceutical Division, LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA075622
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsFAMOTIDINE (10 mg/mL)
Marketing started20200810
Marketing ended20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).