Strength
16 mg/1
Manufacturer
Teva Pharmaceuticals USA Inc.NDC
00093807656
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
5/21/2025
Active Ingredients
TIAGABINE HYDROCHLORIDEApproval Type
Authorized Generic (NDA)
FDA Application
NDA020646On Market Since
3/9/2018
Pharmacological Classes
Anti-epileptic Agent
Decreased Central Nervous System Disorganized Electrical Activity
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