Visitor Monitoring Drug Details: XELODA
 
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Drug Details

Drug Name: XELODA
FDA Application No: (NDA) 020896
Active Ingredient(s): CAPECITABINE
Company: HLR
Original Approval or Tentative Approval Date: April 30, 1998
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
 
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
XELODA CAPECITABINE150MGTABLET; ORAL Prescription No None
XELODA CAPECITABINE500MGTABLET; ORAL Prescription Yes None


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