FDA NDC Directory · JSON-LD · Markdown

Care One Ibuprofen PM

NDC 41520-050 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namediphenhydramine citrate and ibuprofen
Labeler / ManufacturerAmerican Sales Company
Marketing categoryAbbreviated NDA (generic) · App ANDA079113
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDIPHENHYDRAMINE CITRATE (38 mg/1)
IBUPROFEN (200 mg/1)
Marketing started20090220
Package count3

External sources

Source: openFDA. Public-domain (CC0).