Divalproex Sodium 17856-0797

Product NDC

17856-0797

Manufacturer: Atlantic Biologicals Corp.
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)

17856-0797-01

100 POUCH in 1 BOX, UNIT-DOSE (17856-0797-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH

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