Divalproex Sodium 68001-0472-03

Package NDC

68001-0472-03

Manufacturer: Bluepoint Laboratories
Dosage Form: Tablet, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 20, 2021
Listing Expires: December 31, 2027
Application: ANDA079163

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Active Ingredients

Ingredient	Strength
Divalproex Sodium	125 mg/1

Drug Class

Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]

Selected Package

68001-0472-03Selected

500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-03)

Other packages for this product(1)

68001-0472-00

100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-00)

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