Depakote - 21695-163-15 - (Divalproex sodium)

Alphabetical Index


Drug Information of Depakote

Product NDC: 21695-163
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: 21695-163
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021168
Marketing Category: NDA
Start Marketing Date: 20100607

Package Information of Depakote

Package NDC: 21695-163-15
Package Description: 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-163-15)

NDC Information of Depakote

NDC Code 21695-163-15
Proprietary Name Depakote
Package Description 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-163-15)
Product NDC 21695-163
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Divalproex sodium
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100607
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
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