NDCFind

Divalproex Sodium 70518-2626

Product NDC

70518-2626
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

IngredientStrength
Divalproex Sodium500 mg/1

Drug Class

Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]

Packaging Options(1)

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