Strength
50 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
62756025902
Classification
Generic
Dosage Form
CAPSULE
Route
ORAL
Last Updated
2/18/2026
Active Ingredients
ZONISAMIDEApproval Type
Generic (ANDA)
FDA Application
ANDA077634On Market Since
3/17/2006
Pharmacological Classes
Anti-epileptic Agent
Carbonic Anhydrase Inhibitors
Decreased Central Nervous System Disorganized Electrical Activity
P-Glycoprotein Inhibitors
Sulfonamides
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