FDA NDC Directory · JSON-LD · Markdown

acid reducer

NDC 69842-659 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namefamotidine
Labeler / ManufacturerCVS Pharmacy
Marketing categoryAbbreviated NDA (generic) · App ANDA077351
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20220404
Package count2

External sources

Source: openFDA. Public-domain (CC0).