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Divalproex Sodium - 29300-138-10 - (Divalproex Sodium)

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Drug Information of Divalproex Sodium

Product NDC: 29300-138
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: 29300-138
Labeler Name: Unichem Pharmaceuticals (USA), Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079163
Marketing Category: ANDA
Start Marketing Date: 20111001

Package Information of Divalproex Sodium

Package NDC: 29300-138-10
Package Description: 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-10)

NDC Information of Divalproex Sodium

NDC Code 29300-138-10
Proprietary Name Divalproex Sodium
Package Description 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-10)
Product NDC 29300-138
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Divalproex Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20111001
Marketing Category Name ANDA
Labeler Name Unichem 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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