Divalproex Sodium 70518-2626-02

Package NDC

70518-2626-02

Manufacturer: Remedyrepack Inc.
Dosage Form: Tablet, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 13, 2020
Listing Expires: December 31, 2027
Application: ANDA079163

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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

70518-2626-02Selected

30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2626-2)