FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 82461-724 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMedcore LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202413
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (600 mg/1)
Marketing started20261010
Package count1

External sources

Source: openFDA. Public-domain (CC0).