FDA NDC Directory · JSON-LD · Markdown

dual pain reliever

NDC 0363-5220 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameAcetaminophen, Ibuprofen
Labeler / ManufacturerWalgreen Company
Marketing categoryAbbreviated NDA (generic) · App ANDA214836
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsACETAMINOPHEN (250 mg/1)
IBUPROFEN (125 mg/1)
Marketing started20230310
Package count4

External sources

Source: openFDA. Public-domain (CC0).