FDA NDC Directory · JSON-LD · Markdown

Riluzole

NDC 67877-286 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204048
Dosage form / routeTABLET · ORAL
Active ingredientsRILUZOLE (50 mg/1)
Marketing started20160331
Package count5

External sources

Source: openFDA. Public-domain (CC0).