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Divalproex Sodium - 49349-238-02 - (Divalproex Sodium)

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Drug Information of Divalproex Sodium

Product NDC: 49349-238
Proprietary Name: Divalproex Sodium
Non Proprietary Name: Divalproex Sodium
Active Ingredient(s): 125    mg/1 & nbsp;   Divalproex Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Divalproex Sodium

Product NDC: 49349-238
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078790
Marketing Category: ANDA
Start Marketing Date: 20110318

Package Information of Divalproex Sodium

Package NDC: 49349-238-02
Package Description: 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-238-02)

NDC Information of Divalproex Sodium

NDC Code 49349-238-02
Proprietary Name Divalproex Sodium
Package Description 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-238-02)
Product NDC 49349-238
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Divalproex Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110318
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name DIVALPROEX SODIUM
Strength Number 125
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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