NDCFind

Divalproex Sodium 50090-7121

Product NDC

50090-7121
Manufacturer
A-S Medication Solutions
Dosage Form
Tablet, Delayed Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
October 24, 2014
Listing Expires
December 31, 2026
Application
ANDA090554
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Active Ingredients

IngredientStrength
Divalproex Sodium125 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 (50090-7121-0)