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dual action pain reliever

NDC 83324-178 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameAcetaminophen and Ibuprofen
Labeler / ManufacturerCHAIN DRUG MARKETING ASSOCIATION INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA216999
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsACETAMINOPHEN (250 mg/1)
IBUPROFEN (125 mg/1)
Marketing started20241003
Package count1

External sources

Source: openFDA. Public-domain (CC0).