Visitor Monitoring Drug History: ZITHROMAX
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: ZITHROMAX
FDA Application No: (NDA) 050711
Active Ingredient(s): AZITHROMYCIN
Company: PFIZER
 
Label History
 
View the label approved on January 22, 2004 for ZITHROMAX, (NDA) 050711


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/15/2004 017Labeling Revision Letter
Label 
12/18/2003 016Labeling Revision Letter 
1/15/2004 015Labeling Revision Letter
Label 
5/20/2002 013Package Change  
7/22/2002 012Labeling Revision Letter 
12/10/2001 010Manufacturing Change or Addition  
5/24/2002 009Labeling Revision Letter
Label
Review 
10/16/2002 008Labeling Revision Letter 
2/9/2000 007Manufacturing Change or Addition  
11/11/2000 006Labeling Revision  
12/6/1999 005Package Change  
11/22/1999 004Manufacturing Change or Addition  
10/6/1999 003Manufacturing Change or Addition  
7/15/1999 002Manufacturing Change or Addition  
5/16/1997 001Control Supplement  
7/18/1996 000Approval Review 
 
Therapeutic Equivalents
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