Visitor Monitoring Drug History: ZOMETA
 
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: ZOMETA
FDA Application No: (NDA) 021223
Active Ingredient(s): ZOLEDRONIC ACID
Company: NOVARTIS
 
Label History
 
View the label approved on May 26, 2006 for ZOMETA, (NDA) 021223


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
5/25/2006 012Labeling Revision Letter
Label 
10/11/2005 011Labeling Revision Letter
Label 
1/31/2005 010Labeling Revision Letter
Label 
1/31/2005 009Labeling Revision Letter
Label 
3/24/2004 008Labeling Revision Letter
Label 
2/27/2004 006Labeling Revision Letter
Label 
3/7/2003 004Formulation Revision Letter
Label 
2/22/2002 003Labeling Revision Letter
Label
Review 
5/13/2002 002Manufacturing Change or Addition  
2/12/2002 001Manufacturing Change or Addition  
8/20/2001 000Approval Letter
Label
Review
Consumer Information Sheet 
 
Therapeutic Equivalents
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