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DUAL ACTION BACK PAIN RELIEVER

NDC 79481-0152 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameacetaminophen, ibuprofen
Labeler / ManufacturerMeijer, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214836
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsACETAMINOPHEN (250 mg/1)
IBUPROFEN (125 mg/1)
Marketing started20260305
Package count1

External sources

Source: openFDA. Public-domain (CC0).