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DIVALPROEX SODIUM - 55648-725-02 - (DIVALPROEX SODIUM)

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Drug Information of DIVALPROEX SODIUM

Product NDC: 55648-725
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: 55648-725
Labeler Name: WOCKHARDT LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078705
Marketing Category: ANDA
Start Marketing Date: 20090804

Package Information of DIVALPROEX SODIUM

Package NDC: 55648-725-02
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-725-02)

NDC Information of DIVALPROEX SODIUM

NDC Code 55648-725-02
Proprietary Name DIVALPROEX SODIUM
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-725-02)
Product NDC 55648-725
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 WOCKHARDT LIMITED
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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