Visitor Monitoring Drug History: ZYRTEC
 
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Label and Approval History

Drug Name: ZYRTEC
FDA Application No: (NDA) 021621
Active Ingredient(s): CETIRIZINE HYDROCHLORIDE
Company: PFIZER
 
Label History
 
Labels are not available on this site for ZYRTEC, (NDA) 021621
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/16/2004 000Approval Letter
Review 
 
Therapeutic Equivalents
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