FDA NDC Directory · JSON-LD · Markdown

Dalfampridine

NDC 63629-9450 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA206765
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsDALFAMPRIDINE (10 mg/1)
Marketing started20180731
Package count1

External sources

Source: openFDA. Public-domain (CC0).