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FAMOTIDINE

NDC 68382-444 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Generic namefamotidine
Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091020
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsFAMOTIDINE (40 mg/5mL)
Marketing started20210422
Package count1

External sources

Source: openFDA. Public-domain (CC0).