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Divalproex Sodium Delayed Release - 49349-197-02 - (Divalproex Sodium Delayed Release)

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Drug Information of Divalproex Sodium Delayed Release

Product NDC: 49349-197
Proprietary Name: Divalproex Sodium Delayed Release
Non Proprietary Name: Divalproex Sodium Delayed Release
Active Ingredient(s): 250    mg/1 & nbsp;   Divalproex Sodium Delayed Release
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Divalproex Sodium Delayed Release

Product NDC: 49349-197
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078597
Marketing Category: ANDA
Start Marketing Date: 20110420

Package Information of Divalproex Sodium Delayed Release

Package NDC: 49349-197-02
Package Description: 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-197-02)

NDC Information of Divalproex Sodium Delayed Release

NDC Code 49349-197-02
Proprietary Name Divalproex Sodium Delayed Release
Package Description 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-197-02)
Product NDC 49349-197
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Divalproex Sodium Delayed Release
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110420
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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 Delayed Release


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