Visitor Monitoring Drug Details: RABEPRAZOLE SODIUM
 
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Drug Details

Drug Name: RABEPRAZOLE SODIUM
FDA Application No: (ANDA) 076822
Active Ingredient(s): RABEPRAZOLE SODIUM
Company: TEVA
Original Approval or Tentative Approval Date: February 21, 2007
 
 
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
RABEPRAZOLE SODIUM RABEPRAZOLE SODIUM20MGTABLET, DELAYED RELEASE; ORAL Prescription No AB


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