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Divalproex Sodium - 63739-554-10 - (Divalproex Sodium)

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Drug Information of Divalproex Sodium

Product NDC: 63739-554
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: 63739-554
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078853
Marketing Category: ANDA
Start Marketing Date: 20120123

Package Information of Divalproex Sodium

Package NDC: 63739-554-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-554-10) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Divalproex Sodium

NDC Code 63739-554-10
Proprietary Name Divalproex Sodium
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-554-10) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 63739-554
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 20120123
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
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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