Visitor Monitoring Drug Details: DIVALPROEX SODIUM
 
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Drug Details

Drug Name: DIVALPROEX SODIUM
FDA Application No: (ANDA) 078182
Active Ingredient(s): DIVALPROEX SODIUM
Company: UPSHER SMITH
Original Approval or Tentative Approval Date: April 11, 2007
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
DIVALPROEX SODIUM DIVALPROEX SODIUM125MGTABLET, DELAYED RELEASE; ORAL Tentative Approval No None
DIVALPROEX SODIUM DIVALPROEX SODIUM250MGTABLET, DELAYED RELEASE; ORAL Tentative Approval No None
DIVALPROEX SODIUM DIVALPROEX SODIUM500MGTABLET, DELAYED RELEASE; ORAL Tentative Approval No None


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