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Divalproex Sodium - 0615-7555-05 - (divalproex sodium)

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Drug Information of Divalproex Sodium

Product NDC: 0615-7555
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, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Divalproex Sodium

Product NDC: 0615-7555
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077567
Marketing Category: ANDA
Start Marketing Date: 20100208

Package Information of Divalproex Sodium

Package NDC: 0615-7555-05
Package Description: 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-7555-05)

NDC Information of Divalproex Sodium

NDC Code 0615-7555-05
Proprietary Name Divalproex Sodium
Package Description 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-7555-05)
Product NDC 0615-7555
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name divalproex sodium
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100208
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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