Divalproex Sodium 00832-7122-15

Package NDC

00832-7122-15

Manufacturer: Upsher-Smith Laboratories, Llc
Dosage Form: Tablet, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 21, 2014
Application: ANDA078182

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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

00832-7122-15Selected

500 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7122-15)

Other packages for this product(1)

00832-7122-11

100 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7122-11)

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