Strength
125 mg/1
Manufacturer
Upsher-Smith Laboratories LLCNDC
00832712211
Classification
Generic
Dosage Form
TABLET, DELAYED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
DIVALPROEX SODIUMApproval Type
Generic (ANDA)
FDA Application
ANDA078182On Market Since
3/21/2014
Pharmacological Classes
Anti-epileptic Agent
Decreased Central Nervous System Disorganized Electrical Activity
Mood Stabilizer
DIVALPROEX SOD DR 125 MG TAB
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