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Divalproex Sodium - 0115-6911-19 - (DIVALPROEX SODIUM)

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Drug Information of Divalproex Sodium

Product NDC: 0115-6911
Proprietary Name: Divalproex Sodium
Non Proprietary Name: DIVALPROEX SODIUM
Active Ingredient(s): 250    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: 0115-6911
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078791
Marketing Category: ANDA
Start Marketing Date: 20090804

Package Information of Divalproex Sodium

Package NDC: 0115-6911-19
Package Description: 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6911-19)

NDC Information of Divalproex Sodium

NDC Code 0115-6911-19
Proprietary Name Divalproex Sodium
Package Description 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6911-19)
Product NDC 0115-6911
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 20090804
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories Inc.
Substance Name DIVALPROEX SODIUM
Strength Number 250
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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