Visitor Monitoring Drug History: ZETIA
 
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: ZETIA
FDA Application No: (NDA) 021445
Active Ingredient(s): EZETIMIBE
Company: MSP SINGAPORE
 
Label History
 
View the label approved on November 6, 2006 for ZETIA, (NDA) 021445


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
11/2/2006 016Labeling Revision Letter
Label 
3/16/2006 015Labeling Revision Letter
Label 
1/19/2006 014Labeling Revision Letter
Label 
5/23/2006 013New or Modified Indication Letter
Label 
3/16/2006 012Efficacy Supplement with Clinical Data to Support Letter
Label 
3/22/2005 011Labeling Revision Letter
Label 
3/2/2005 007Labeling Revision Letter
Label 
9/22/2004 006Labeling Revision Letter 
7/23/2004 004Labeling Revision Letter
Label 
7/23/2004 003Labeling Revision Letter
Label 
7/23/2004 001Labeling Revision Letter
Label 
10/25/2002 000Approval Letter
Label
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