Divalproex Sodium 68084-0782-61

Package NDC

68084-0782-61

Manufacturer: American Health Packaging
Dosage Form: Tablet, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 26, 2016
Listing Expires: December 31, 2026
Application: ANDA090554

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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

68084-0782-61Selected

90 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-782-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-782-11)