Divalproex Sodium 67046-1631-03

Package NDC

67046-1631-03

Manufacturer: Coupler Llc
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: December 24, 2025
Listing Expires: December 31, 2026
Application: ANDA214643

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Active Ingredients

Ingredient	Strength
Divalproex Sodium	500 mg/1

Drug Class

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

Selected Package

67046-1631-03Selected

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (67046-1631-3)