NDCFind

Divalproex Sodium 68788-8609-03

Package NDC

68788-8609-03

Product NDC: 68788-8609

Manufacturer
Preferred Pharmaceuticals Inc.
Dosage Form
Tablet, Delayed Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
March 28, 2025
Listing Expires
December 31, 2027
Application
ANDA078597
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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]

Selected Package

68788-8609-03Selected

30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8609-3)

Other packages for this product(2)

60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8609-6)

90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8609-9)