FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 53746-137 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA071935
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
Marketing started20090105
Package count6

External sources

Source: openFDA. Public-domain (CC0).