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Acetaminophen and Ibuprofen

NDC 58602-893 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurohealth LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218359
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsACETAMINOPHEN (250 mg/1)
IBUPROFEN (125 mg/1)
Marketing started20240326
Package count30

External sources

Source: openFDA. Public-domain (CC0).