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Divalproex Sodium - 21695-819-90 - (Divalproex Sodium)

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Drug Information of Divalproex Sodium

Product NDC: 21695-819
Proprietary Name: Divalproex Sodium
Non Proprietary Name: Divalproex Sodium
Active Ingredient(s): 500    mg/1 & nbsp;   Divalproex Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Divalproex Sodium

Product NDC: 21695-819
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078790
Marketing Category: ANDA
Start Marketing Date: 20091014

Package Information of Divalproex Sodium

Package NDC: 21695-819-90
Package Description: 90 TABLET, DELAYED RELEASE in 1 BOTTLE (21695-819-90)

NDC Information of Divalproex Sodium

NDC Code 21695-819-90
Proprietary Name Divalproex Sodium
Package Description 90 TABLET, DELAYED RELEASE in 1 BOTTLE (21695-819-90)
Product NDC 21695-819
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Divalproex Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20091014
Marketing Category Name ANDA
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 Divalproex Sodium


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