Discontinued
Strength
600 mg/1
Manufacturer
Mylan Pharmaceuticals Inc.NDC
51525043101
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
FELBAMATEApproval Type
Authorized Generic (NDA)
FDA Application
NDA020189On Market Since
11/11/2011
Pharmacological Classes
Anti-epileptic Agent
Decreased Central Nervous System Disorganized Electrical Activity
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