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Divalproex Sodium - 68180-266-01 - (Divalproex Sodium)

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Drug Information of Divalproex Sodium

Product NDC: 68180-266
Proprietary Name: Divalproex Sodium
Non Proprietary Name: Divalproex Sodium
Active Ingredient(s): 250    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: 68180-266
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078790
Marketing Category: ANDA
Start Marketing Date: 20080729

Package Information of Divalproex Sodium

Package NDC: 68180-266-01
Package Description: 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68180-266-01)

NDC Information of Divalproex Sodium

NDC Code 68180-266-01
Proprietary Name Divalproex Sodium
Package Description 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68180-266-01)
Product NDC 68180-266
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 Lupin Pharmaceuticals, 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


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