Divalproex Sodium 31722-0021

Product NDC

31722-0021

Manufacturer: Camber Pharmaceuticals, Inc.
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: September 23, 2023
Listing Expires: December 31, 2026
Application: ANDA215527

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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)

31722-0021-01

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-021-01)

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31722-0021-05

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-021-05)

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