FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 68016-801 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerChain Drug Consortium, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077367
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20211101
Package count1

External sources

Source: openFDA. Public-domain (CC0).