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Ibuprofen

NDC 67877-321 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091625
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
Marketing started20151221
Package count5

External sources

Source: openFDA. Public-domain (CC0).