FDA NDC Directory · JSON-LD · Markdown

ibuprofen pm

NDC 30142-050 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namediphenhydramine citrate, ibuprofen
Labeler / ManufacturerKroger Company
Marketing categoryAbbreviated NDA (generic) · App ANDA079113
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDIPHENHYDRAMINE CITRATE (38 mg/1)
IBUPROFEN (200 mg/1)
Marketing started20090406
Package count2

External sources

Source: openFDA. Public-domain (CC0).