FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 73614-201 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBrisk Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA202413
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
Marketing started20240523
Package count1

External sources

Source: openFDA. Public-domain (CC0).