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Divalproex sodium - 0615-1393-31 - (Divalproex sodium)

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Drug Information of Divalproex sodium

Product NDC: 0615-1393
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): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Divalproex sodium

Product NDC: 0615-1393
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078979
Marketing Category: ANDA
Start Marketing Date: 20090123

Package Information of Divalproex sodium

Package NDC: 0615-1393-31
Package Description: 31 CAPSULE in 1 BLISTER PACK (0615-1393-31)

NDC Information of Divalproex sodium

NDC Code 0615-1393-31
Proprietary Name Divalproex sodium
Package Description 31 CAPSULE in 1 BLISTER PACK (0615-1393-31)
Product NDC 0615-1393
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Divalproex sodium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090123
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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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