FDA NDC Directory · JSON-LD · Markdown

Maximum Strength Acid Reducer

NDC 49483-720 · HUMAN OTC DRUG · TABLET

Generic nameFamotidine
Labeler / ManufacturerTIME CAP LABORATORIES,INC
Marketing categoryAbbreviated NDA (generic) · App ANDA217543
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (20 mg/1)
Marketing started20230615
Package count2

External sources

Source: openFDA. Public-domain (CC0).