NDCFind

Divalproex Sodium 67046-1571

Product NDC

67046-1571
Manufacturer
Coupler Llc
Dosage Form
Tablet, Delayed Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
July 2, 2025
Listing Expires
December 31, 2026
Application
ANDA078597
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Active Ingredients

IngredientStrength
Divalproex Sodium250 mg/1

Drug Class

Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]

Packaging Options(1)

30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1571-3)