FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN

NDC 58602-913 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerAurohealth LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208865
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20260928
Package count2

External sources

Source: openFDA. Public-domain (CC0).