FDA NDC Directory · JSON-LD · Markdown

ibuprofen

NDC 71335-2068 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIbuprofen
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA072096
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started19940816
Package count10

External sources

Source: openFDA. Public-domain (CC0).