FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 72559-038 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerLittle Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215766
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (10 mg/10mg)
Marketing started20250515
Package count1

External sources

Source: openFDA. Public-domain (CC0).