Visitor Monitoring Drug Details: FEXOFENADINE
 
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Drug Details

Drug Name: FEXOFENADINE
FDA Application No: (ANDA) 077081
Active Ingredient(s): FEXOFENADINE HYDROCHLORIDE
Company: MYLAN
Original Approval or Tentative Approval Date: April 16, 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
FEXOFENADINE FEXOFENADINE HYDROCHLORIDE60MGTABLET; ORAL Tentative Approval No None
FEXOFENADINE FEXOFENADINE HYDROCHLORIDE180MGTABLET; ORAL Prescription No None
FEXOFENADINE HYDROCHLORIDE FEXOFENADINE HYDROCHLORIDE180MGTABLET; ORAL Prescription No AB


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