Divalproex Sodium 65162-0755

Product NDC

65162-0755

Manufacturer: Amneal Pharmaceuticals Llc
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 1, 2015
Listing Expires: December 31, 2027
Application: ANDA203730

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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]

Packaging Options(2)

65162-0755-10

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-755-10)

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65162-0755-50

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-755-50)

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