FDA NDC Directory · JSON-LD · Markdown

Medline

NDC 53329-603 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIburprofen
Labeler / ManufacturerMedline Industries, LP
Marketing categoryAbbreviated NDA (generic) · App ANDA072096
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20260828
Package count1

External sources

Source: openFDA. Public-domain (CC0).