Strength
4 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
62756022483
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
2/18/2026
Active Ingredients
TIAGABINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA077555On Market Since
11/4/2011
Pharmacological Classes
Anti-epileptic Agent
Decreased Central Nervous System Disorganized Electrical Activity
Generic Alternatives
No alternatives available
No alternatives found with the same active ingredient, strength, and dosage form.
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