FDA NDC Directory · JSON-LD · Markdown

Rufinamide

NDC 72603-261 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Labeler / ManufacturerNorthStar RxLLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216841
Dosage form / routeSUSPENSION · ORAL
Active ingredientsRUFINAMIDE (40 mg/mL)
Marketing started20240801
Package count1

External sources

Source: openFDA. Public-domain (CC0).