Strength
150 mg/1
Manufacturer
Breckenridge Pharmaceutical Inc.NDC
51991029201
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
OXCARBAZEPINEApproval Type
Generic (ANDA)
FDA Application
ANDA078069On Market Since
1/11/2008
Pharmacological Classes
Anti-epileptic Agent
Decreased Central Nervous System Disorganized Electrical Activity
OXCARBAZEPINE 150 MG TABLET
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OXCARBAZEPINE ER 150 MG TABLET
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