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divalproex sodium - 68382-106-10 - (divalproex sodium)

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Drug Information of divalproex sodium

Product NDC: 68382-106
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): CAPSULE, COATED PELLETS
Coding System: National Drug Codes(NDC)

Labeler Information of divalproex sodium

Product NDC: 68382-106
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078919
Marketing Category: ANDA
Start Marketing Date: 20090127

Package Information of divalproex sodium

Package NDC: 68382-106-10
Package Description: 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-106-10)

NDC Information of divalproex sodium

NDC Code 68382-106-10
Proprietary Name divalproex sodium
Package Description 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-106-10)
Product NDC 68382-106
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name divalproex sodium
Dosage Form Name CAPSULE, COATED PELLETS
Route Name ORAL
Start Marketing Date 20090127
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) 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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