Divalproex Sodium 29300-0381

Product NDC

29300-0381

Manufacturer: Unichem Pharmaceuticals (usa), Inc.
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: February 25, 2022
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(2)

29300-0381-01

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-381-01)

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29300-0381-05

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-381-05)

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