Visitor Monitoring Drug History: EFFEXOR
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: EFFEXOR
FDA Application No: (NDA) 020151
Active Ingredient(s): VENLAFAXINE HYDROCHLORIDE
Company: WYETH PHARMS INC
 
Label History
 
View the label approved on September 26, 2007 for EFFEXOR, (NDA) 020151


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
9/20/2007 049Labeling Revision Letter
Label 
9/20/2007 047Labeling Revision Letter
Label 
8/1/2007 046Labeling Revision Letter
Label 
10/20/2006 045Labeling Revision Letter
Label 
9/14/2006 044Labeling Revision Letter
Label 
2/7/2007 043Labeling Revision Letter
Label 
1/12/2006 039Labeling Revision Letter 
1/12/2006 038Labeling Revision Letter 
2/18/2005 035Labeling Revision Letter 
2/24/2006 034Labeling Revision Letter 
8/1/2007 033Labeling Revision Label 
5/13/2004 032Labeling Revision Letter
Label 
5/13/2004 030Labeling Revision Letter
Label 
4/8/2004 029Labeling Revision Letter 
5/13/2004 028Labeling Revision Letter
Label 
3/19/2004 027Labeling Revision Letter 
1/31/2003 025Supplement Review 
5/5/2004 024Patient Population Altered Letter 
1/31/2003 023Supplement Review 
1/31/2003 022Supplement Review 
1/31/2003 021Supplement Review 
1/31/2003 020Supplement Review 
1/31/2003 019Supplement Review 
5/2/2001 018New or Modified Indication Letter
Label
Review 
5/2/2001 017New or Modified Indication Letter
Label
Review 
1/31/2003 016Supplement Review 
7/20/2000 015Labeling Revision  
3/3/2000 014Labeling Revision  
7/20/2000 013Labeling Revision  
10/4/1999 012Control Supplement  
7/20/2000 011Labeling Revision  
12/9/1998 009Labeling Revision  
12/9/1998 008Labeling Revision  
12/9/1998 007Labeling Revision  
12/9/1998 006Labeling Revision  
6/25/1996 005Labeling Revision  
11/16/1994 003Control Supplement  
11/28/1994 002Labeling Revision  
11/16/1994 001Control Supplement  
12/28/1993 000Approval Other Important Information from FDA 
 
There are no Therapeutic Equivalents
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