Divalproex Sodium 70518-4553

Product NDC

70518-4553

Manufacturer: Remedyrepack Inc.
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 21, 2026
Listing Expires: December 31, 2027
Application: ANDA214643

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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]

Packaging Options(1)

70518-4553-00

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4553-0)

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