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Ibuprofen PM

NDC 0363-0050 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namediphenhydramine citrate, ibuprofen
Labeler / ManufacturerWalgreen Company
Marketing categoryAbbreviated NDA (generic) · App ANDA079113
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDIPHENHYDRAMINE CITRATE (38 mg/1)
IBUPROFEN (200 mg/1)
Marketing started20090219
Package count5

External sources

Source: openFDA. Public-domain (CC0).