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Ibuprofen and Famotidine

NDC 80425-0587 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218684
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
FAMOTIDINE (26.6 mg/1)
Marketing started20260618
Package count3

External sources

Source: openFDA. Public-domain (CC0).