FDA NDC Directory · JSON-LD · Markdown

IBU

NDC 71205-604 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameIbuprofen
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA075682
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (400 mg/1)
Marketing started20081120
Package count7

External sources

Source: openFDA. Public-domain (CC0).