Visitor Monitoring Drug History: FLOVENT
 
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: FLOVENT
FDA Application No: (NDA) 020549
Active Ingredient(s): FLUTICASONE PROPIONATE
Company: GLAXOSMITHKLINE
 
Label History
 
View the label approved on April 5, 2004 for FLOVENT, (NDA) 020549


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
3/26/2004 016Labeling Revision Letter
Label 
10/8/2003 014Labeling Revision Letter
Label
Review 
6/20/2003 012Labeling Revision Letter
Label 
8/27/2001 010Control Supplement  
11/1/2000 009Control Supplement  
3/29/2001 008Labeling Revision  
5/17/2000 007Control Supplement  
7/19/1999 006Labeling Revision Review 
4/23/1999 004Control Supplement  
1/19/2001 003Control Supplement  
12/22/1998 002Labeling Revision Review 
12/3/1998 001Control Supplement  
11/7/1997 000Approval Review 
 
There are no Therapeutic Equivalents
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