Divalproex Sodium 55111-0529-05

Package NDC

55111-0529-05

Manufacturer: Dr.reddy's Laboratories Limited
Dosage Form: Tablet, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 29, 2008
Listing Expires: December 31, 2026
Application: ANDA078755

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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

55111-0529-05Selected

500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-529-05)

Other packages for this product(3)

55111-0529-01

100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-529-01)

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55111-0529-30

30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-529-30)

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55111-0529-78

10 BLISTER PACK in 1 CARTON (55111-529-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-529-79)

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