FDA NDC Directory · JSON-LD · Markdown

Famotidine

NDC 50090-6790 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA215767
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMOTIDINE (40 mg/1)
Marketing started20211104
Package count2

External sources

Source: openFDA. Public-domain (CC0).