FDA NDC Directory · JSON-LD · Markdown

ibuprofen

NDC 0904-7912 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIbuprofen
Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA072096
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started19940816
Package count2

External sources

Source: openFDA. Public-domain (CC0).