FDA NDC Directory · JSON-LD · Markdown

Maximum Strength Acid Controller

NDC 21130-027 · HUMAN OTC DRUG · TABLET

Generic nameFamotidine
Labeler / ManufacturerBETTER LIVING BRANDS LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA217543
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20230623
Package count1

External sources

Source: openFDA. Public-domain (CC0).