FDA NDC Directory · JSON-LD · Markdown

famotidine

NDC 69230-326 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerCamber Consumer Care Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA215766
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (10 mg/1)
Marketing started20211108
Package count5

External sources

Source: openFDA. Public-domain (CC0).