FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN PM

NDC 21130-623 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namediphenhydramine citrate, ibuprofen
Labeler / ManufacturerSafeway
Marketing categoryAbbreviated NDA (generic) · App ANDA079113
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDIPHENHYDRAMINE CITRATE (38 mg/1)
IBUPROFEN (200 mg/1)
Marketing started20251229
Package count1

External sources

Source: openFDA. Public-domain (CC0).