Visitor Monitoring Drug Details: FEXOFENADINE HYDROCHLORIDE
 
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Drug Details

Drug Name: FEXOFENADINE HYDROCHLORIDE
FDA Application No: (ANDA) 076502
Active Ingredient(s): FEXOFENADINE HYDROCHLORIDE
Company: DR REDDYS LABS LTD
Original Approval or Tentative Approval Date: April 12, 2006
 
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 HYDROCHLORIDE FEXOFENADINE HYDROCHLORIDE30MGTABLET; ORAL Prescription No AB
FEXOFENADINE HYDROCHLORIDE FEXOFENADINE HYDROCHLORIDE60MGTABLET; ORAL Prescription No AB
FEXOFENADINE HYDROCHLORIDE FEXOFENADINE HYDROCHLORIDE180MGTABLET; ORAL Prescription No AB


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