FDA NDC Directory · JSON-LD · Markdown

Curist Acid Relief

NDC 72559-032 · HUMAN OTC DRUG · TABLET

Generic nameFamotidine 20 mg
Labeler / ManufacturerLittle Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215822
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20240131
Package count1

External sources

Source: openFDA. Public-domain (CC0).