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Divalproex Sodium - 52125-048-02 - (Divalproex Sodium)

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Drug Information of Divalproex Sodium

Product NDC: 52125-048
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: 52125-048
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078445
Marketing Category: ANDA
Start Marketing Date: 20130228

Package Information of Divalproex Sodium

Package NDC: 52125-048-02
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-048-02)

NDC Information of Divalproex Sodium

NDC Code 52125-048-02
Proprietary Name Divalproex Sodium
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-048-02)
Product NDC 52125-048
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 20130228
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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