FDA NDC Directory · JSON-LD · Markdown

Acid Reducer Maximum Strength

NDC 85828-443 · HUMAN OTC DRUG · TABLET

Generic nameFamotidine 20mg
Labeler / ManufacturerGrocery Outlet
Marketing categoryAbbreviated NDA (generic) · App ANDA215822
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20260320
Package count1

External sources

Source: openFDA. Public-domain (CC0).