FDA NDC Directory · JSON-LD · Markdown

dual action

NDC 11822-5777 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameAcetaminophen, Ibuprofen
Labeler / ManufacturerRite Aid Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA214836
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsACETAMINOPHEN (250 mg/1)
IBUPROFEN (125 mg/1)
Marketing started20230524
Package count3

External sources

Source: openFDA. Public-domain (CC0).