FDA NDC Directory · JSON-LD · Markdown

ibuprofen

NDC 71205-787 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIbuprofen
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA072096
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started19940816
Package count4

External sources

Source: openFDA. Public-domain (CC0).