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Divalproex Sodium - 65862-401-71 - (Divalproex Sodium)

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Drug Information of Divalproex Sodium

Product NDC: 65862-401
Proprietary Name: Divalproex Sodium
Non Proprietary Name: Divalproex Sodium
Active Ingredient(s): 125    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: 65862-401
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090554
Marketing Category: ANDA
Start Marketing Date: 20110421

Package Information of Divalproex Sodium

Package NDC: 65862-401-71
Package Description: 7000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-401-71)

NDC Information of Divalproex Sodium

NDC Code 65862-401-71
Proprietary Name Divalproex Sodium
Package Description 7000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-401-71)
Product NDC 65862-401
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Divalproex Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110421
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name DIVALPROEX SODIUM
Strength Number 125
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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