FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 0904-7588 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA071268
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (600 mg/1)
Marketing started20251103
Package count2

External sources

Source: openFDA. Public-domain (CC0).