Divalproex Sodium 87441-0028

Product NDC

87441-0028

Manufacturer: Unit Dose Solutions, Inc.
Dosage Form: Tablet, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 17, 2026
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]

Packaging Options(1)

87441-0028-01

30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (87441-028-01)

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