FDA NDC Directory · JSON-LD · Markdown

Rolaids ACID DEFENSE

NDC 84126-367 · HUMAN OTC DRUG · TABLET

Generic nameFamotitine
Labeler / ManufacturerThe Procter & Gamble Manufacturing Company
Marketing categoryAbbreviated NDA (generic) · App ANDA077351
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20250901
Package count1

External sources

Source: openFDA. Public-domain (CC0).