FDA NDC Directory · JSON-LD · Markdown

riluzole

NDC 68462-381 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA091394
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRILUZOLE (50 mg/1)
Marketing started20130618
Package count2

External sources

Source: openFDA. Public-domain (CC0).