FDA NDC Directory · JSON-LD · Markdown

PEPCID AC Maximum Strength

NDC 16837-855 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameFamotidine
Labeler / ManufacturerKenvue Brands LLC
Marketing categoryNew Drug Application (innovator) · App NDA020325
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20030901
Package count18

External sources

Source: openFDA. Public-domain (CC0).