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IBUPROFEN AND FAMOTIDINE

NDC 85509-1315 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameIbuprofen and famotidine
Labeler / ManufacturerPHOENIX RX LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216814
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (26.6 mg/1)
IBUPROFEN (800 mg/1)
Marketing started20230315
Package count3

External sources

Source: openFDA. Public-domain (CC0).