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Ibuprofen and Famotidine

NDC 70771-1924 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218684
Dosage form / routeTABLET · ORAL
Active ingredientsFAMOTIDINE (26.6 mg/1)
IBUPROFEN (800 mg/1)
Marketing started20250601
Package count1

External sources

Source: openFDA. Public-domain (CC0).