NDCFind

Divalproex Sodium 82804-0233

Product NDC

82804-0233
Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Delayed Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
June 26, 2024
Listing Expires
December 31, 2026
Application
ANDA078853
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Active Ingredients

IngredientStrength
Divalproex Sodium250 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 BOTTLE (82804-233-30)