FDA NDC Directory · JSON-LD · Markdown

ibuprofen

NDC 0363-0604 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIbuprofen
Labeler / ManufacturerWalgreen Company
Marketing categoryAbbreviated NDA (generic) · App ANDA072096
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20090121
Package count5

External sources

Source: openFDA. Public-domain (CC0).