FDA NDC Directory · JSON-LD · Markdown

Acid Reducer Maximum Strength

NDC 43598-960 · HUMAN OTC DRUG · TABLET

Generic nameFamotidine
Labeler / ManufacturerDr.Reddys Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077367
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20200901
Package count3

External sources

Source: openFDA. Public-domain (CC0).