FDA NDC Directory · JSON-LD · Markdown

FAMOTIDINE

NDC 43602-602 · HUMAN OTC DRUG · TABLET

Generic nameFamotidine
Labeler / ManufacturerAscent Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216030
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20211103
Package count2

External sources

Source: openFDA. Public-domain (CC0).