Divalproex Sodium 17856-0109-01

Package NDC

17856-0109-01

Manufacturer: Atlantic Biologicals Corp.
Dosage Form: Capsule, Coated Pellets
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 31, 2019
Listing Expires: December 31, 2026
Application: ANDA078919

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Active Ingredients

Ingredient	Strength
Divalproex Sodium	125 mg/1

Drug Class

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

Selected Package

17856-0109-01Selected

100 POUCH in 1 BOX (17856-0109-1) / 1 CAPSULE, COATED PELLETS in 1 POUCH