Visitor Monitoring Drug History: CETIRIZINE
 
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Label and Approval History

Drug Name: CETIRIZINE
FDA Application No: (ANDA) 076581
Active Ingredient(s): CETIRIZINE HYDROCHLORIDE
Company: TEVA
 
Label History
 
Labels are not available on this site for CETIRIZINE, (ANDA) 076581
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/21/2004 000Tentative Approval  
 
Therapeutic Equivalents
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