FDA NDC Directory · JSON-LD · Markdown

Rufinamide

NDC 72205-038 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Labeler / ManufacturerNovadoz Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214817
Dosage form / routeSUSPENSION · ORAL
Active ingredientsRUFINAMIDE (40 mg/mL)
Marketing started20250415
Package count1

External sources

Source: openFDA. Public-domain (CC0).