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Divalproex Sodium - 0615-7533-01 - (Divalproex Sodium)

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Drug Information of Divalproex Sodium

Product NDC: 0615-7533
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: 0615-7533
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078182
Marketing Category: ANDA
Start Marketing Date: 20110121

Package Information of Divalproex Sodium

Package NDC: 0615-7533-01
Package Description: 10 BLISTER PACK in 1 CARTON (0615-7533-01) > 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7533-39)

NDC Information of Divalproex Sodium

NDC Code 0615-7533-01
Proprietary Name Divalproex Sodium
Package Description 10 BLISTER PACK in 1 CARTON (0615-7533-01) > 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7533-39)
Product NDC 0615-7533
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Divalproex Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110121
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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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