Divalproex Sodium 68071-3553

Product NDC

68071-3553

Manufacturer: Nucare Pharmaceuticals,inc.
Dosage Form: Tablet, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 29, 2008
Listing Expires: December 31, 2026
Application: ANDA078597

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Active Ingredients

Ingredient	Strength
Divalproex Sodium	250 mg/1

Drug Class

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

Packaging Options(1)

68071-3553-06

60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3553-6)

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