Visitor Monitoring Drug Details: PANTOPRAZOLE
 
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Drug Details

Drug Name: PANTOPRAZOLE
FDA Application No: (ANDA) 077057
Active Ingredient(s): PANTOPRAZOLE SODIUM
Company: SANDOZ
Original Approval or Tentative Approval Date: April 19, 2006
 
There are no 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
PANTOPRAZOLE PANTOPRAZOLE SODIUM20MGTABLET, DELAYED RELEASE; ORAL Tentative Approval No None
PANTOPRAZOLE PANTOPRAZOLE SODIUM40MGTABLET, DELAYED RELEASE; ORAL Tentative Approval No None


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