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DIVALPROEX SODIUM - 16590-648-60 - (DIVALPROEX SODIUM)

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Drug Information of DIVALPROEX SODIUM

Product NDC: 16590-648
Proprietary Name: DIVALPROEX SODIUM
Non Proprietary Name: DIVALPROEX SODIUM
Active Ingredient(s): 500    mg/1 & nbsp;   DIVALPROEX SODIUM
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE PARTICLES
Coding System: National Drug Codes(NDC)

Labeler Information of DIVALPROEX SODIUM

Product NDC: 16590-648
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078597
Marketing Category: ANDA
Start Marketing Date: 20080729

Package Information of DIVALPROEX SODIUM

Package NDC: 16590-648-60
Package Description: 60 TABLET, DELAYED RELEASE PARTICLES in 1 BOTTLE (16590-648-60)

NDC Information of DIVALPROEX SODIUM

NDC Code 16590-648-60
Proprietary Name DIVALPROEX SODIUM
Package Description 60 TABLET, DELAYED RELEASE PARTICLES in 1 BOTTLE (16590-648-60)
Product NDC 16590-648
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIVALPROEX SODIUM
Dosage Form Name TABLET, DELAYED RELEASE PARTICLES
Route Name ORAL
Start Marketing Date 20080729
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name DIVALPROEX SODIUM
Strength Number 500
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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