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Ibuprofen

NDC 51655-042 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091625
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (600 mg/1)
Marketing started20220909
Package count4

External sources

Source: openFDA. Public-domain (CC0).