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) 050784
Active Ingredient(s): AZITHROMYCIN
Company: PFIZER
 
Label History
 
View the label approved on January 22, 2004 for ZITHROMAX, (NDA) 050784


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 006New or Modified Indication Letter
Label
Review 
12/18/2003 005Labeling Revision Letter 
1/15/2004 004New or Modified Indication Letter
Label
Review 
10/16/2002 002Labeling Revision Letter 
12/17/2002 001Manufacturing Change or Addition  
5/24/2002 000Approval Letter
Label
Review 
 
Therapeutic Equivalents
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