FDA NDC Directory · JSON-LD · Markdown

Ibuprofen Famotidine

NDC 72189-667 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA218684
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
FAMOTIDINE (26.6 mg/1)
Marketing started20260622
Package count1

External sources

Source: openFDA. Public-domain (CC0).