FDA NDC Directory · JSON-LD · Markdown

ACID REDUCER

NDC 51316-511 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameFamotidine
Labeler / ManufacturerCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Marketing categoryAbbreviated NDA (generic) · App ANDA077351
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20260413
Package count1

External sources

Source: openFDA. Public-domain (CC0).