FDA NDC Directory · JSON-LD · Markdown

dual action pain reliever

NDC 69452-447 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameAcetaminophen and Ibuprofen
Labeler / ManufacturerBionpharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216999
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsACETAMINOPHEN (250 mg/1)
IBUPROFEN (125 mg/1)
Marketing started20240808
Package count1

External sources

Source: openFDA. Public-domain (CC0).