Divalproex Sodium 00615-8587-39

Package NDC

00615-8587-39

Manufacturer: Ncs Healthcare Of Ky, Llc Dba Vangard Labs
Dosage Form: Tablet, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 26, 2024
Listing Expires: December 31, 2026
Application: ANDA078853

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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]

Selected Package

00615-8587-39Selected

30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8587-39)