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Divalproex Sodium - 55154-5626-9 - (Divalproex Sodium)

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Drug Information of Divalproex Sodium

Product NDC: 55154-5626
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: 55154-5626
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078182
Marketing Category: ANDA
Start Marketing Date: 20080729

Package Information of Divalproex Sodium

Package NDC: 55154-5626-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-5626-9) > 5 TABLET, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Divalproex Sodium

NDC Code 55154-5626-9
Proprietary Name Divalproex Sodium
Package Description 6 BLISTER PACK in 1 CARTON (55154-5626-9) > 5 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 55154-5626
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Divalproex Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080729
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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