Strength
200 mg/1
Manufacturer
Glenmark Pharmaceuticals Inc., USANDC
68462071308
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
RUFINAMIDEApproval Type
Generic (ANDA)
FDA Application
ANDA205075On Market Since
5/16/2016
Related Drugs
Same classification
No related drugs found.