FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 69396-141 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerTrifecta Pharmaceuticals USA LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207095
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20230808
Package count2

External sources

Source: openFDA. Public-domain (CC0).