FDA NDC Directory · JSON-LD · Markdown

FAMOTIDINE

NDC 67877-842 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215630
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20220708
Package count3

External sources

Source: openFDA. Public-domain (CC0).