Divalproex Sodium 69452-0435-13

Package NDC

69452-0435-13

Manufacturer: Bionpharma Inc.
Dosage Form: Tablet, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 26, 2024
Listing Expires: December 31, 2027
Application: ANDA078853

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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]

Selected Package

69452-0435-13Selected

30 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-13)

Other packages for this product(2)

69452-0435-20

100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-20)

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69452-0435-30

500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-30)

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