Depakote - 0074-7126-13 - (Divalproex Sodium)

Alphabetical Index


Drug Information of Depakote

Product NDC: 0074-7126
Proprietary Name: Depakote
Non Proprietary Name: Divalproex Sodium
Active Ingredient(s): 500    mg/1 & nbsp;   Divalproex Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Depakote

Product NDC: 0074-7126
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021168
Marketing Category: NDA
Start Marketing Date: 20000804

Package Information of Depakote

Package NDC: 0074-7126-13
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-7126-13)

NDC Information of Depakote

NDC Code 0074-7126-13
Proprietary Name Depakote
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-7126-13)
Product NDC 0074-7126
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Divalproex Sodium
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20000804
Marketing Category Name NDA
Labeler Name AbbVie Inc.
Substance Name DIVALPROEX SODIUM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

Complete Information of Depakote


General Information