Visitor Monitoring Drug History: NICODERM CQ
 
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: NICODERM CQ
FDA Application No: (NDA) 020165
Active Ingredient(s): NICOTINE
Company: SANOFI AVENTIS US
 
Label History
 
View the label approved on April 19, 2007 for NICODERM CQ, (NDA) 020165


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
4/13/2007 024Labeling Revision Letter
Label 
9/15/2006 023Labeling Revision Letter
Label 
8/13/2002 020Labeling Revision Letter 
6/8/2001 019Labeling Revision  
9/21/2000 018Manufacturing Change or Addition  
2/16/2000 017Formulation Revision  
2/16/2000 016Labeling Revision  
9/14/1999 015Control Supplement  
8/21/1997 014Manufacturing Change or Addition  
8/21/1997 013Manufacturing Change or Addition  
9/11/1997 012Package Change  
8/2/1996 011OTC Labeling  
1/23/1996 009Package Change  
7/19/1993 006Control Supplement  
7/19/1993 005Control Supplement  
8/12/1992 004Manufacturing Change or Addition  
7/22/1992 003Manufacturing Change or Addition  
7/22/1992 002Manufacturing Change or Addition  
11/7/1991 000Approval  
 
Therapeutic Equivalents
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