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DIVALPROEX SODIUM - 60505-3065-8 - (DIVALPROEX SODIUM)

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Drug Information of DIVALPROEX SODIUM

Product NDC: 60505-3065
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: 60505-3065
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077615
Marketing Category: ANDA
Start Marketing Date: 20080729

Package Information of DIVALPROEX SODIUM

Package NDC: 60505-3065-8
Package Description: 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-3065-8)

NDC Information of DIVALPROEX SODIUM

NDC Code 60505-3065-8
Proprietary Name DIVALPROEX SODIUM
Package Description 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-3065-8)
Product NDC 60505-3065
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIVALPROEX SODIUM
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080729
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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