FDA NDC Directory · JSON-LD · Markdown

Maximum Strength Acid Reducer

NDC 11673-697 · HUMAN OTC DRUG · TABLET

Generic nameFamotidine
Labeler / ManufacturerTARGET CORPORATION
Marketing categoryAbbreviated NDA (generic) · App ANDA217543
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20240515
Package count4

External sources

Source: openFDA. Public-domain (CC0).