FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN

NDC 72288-080 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIbuprofen
Labeler / ManufacturerAmazon.com Services LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA072096
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20260723
Package count1

External sources

Source: openFDA. Public-domain (CC0).