FDA NDC Directory · JSON-LD · Markdown

acid relief

NDC 11822-1194 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameFamotidine
Labeler / ManufacturerRite Aid Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA077351
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20230315
Marketing ended20261231
Package count4

External sources

Source: openFDA. Public-domain (CC0).