Visitor Monitoring Drug History: XANAX
 
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: XANAX
FDA Application No: (NDA) 018276
Active Ingredient(s): ALPRAZOLAM
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for XANAX, (NDA) 018276
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/2/2004 039Labeling Revision Letter
Review 
4/2/2004 038Labeling Revision Letter
Review 
11/7/2002 037Control Supplement  
11/16/1999 036Package Change  
5/2/2000 035Labeling Revision Review 
11/24/1998 034Labeling Revision  
12/20/1996 033Labeling Revision Review 
4/18/1996 032Labeling Revision  
9/14/1993 031Labeling Revision  
12/1/1992 028Labeling Revision  
5/21/1993 027Control Supplement  
9/30/1993 026Manufacturing Change or Addition  
6/22/1994 025Control Supplement  
3/24/1989 022Manufacturing Change or Addition  
10/22/1990 021Labeling Revision  
8/3/1988 020Labeling Revision  
7/26/1988 019Manufacturing Change or Addition  
3/25/1988 018Package Change  
11/6/1990 017New or Modified Indication  
10/23/1990 016Labeling Revision  
11/6/1990 015Labeling Revision  
8/17/1988 014Control Supplement  
2/11/1987 013Labeling Revision  
7/16/1986 012Manufacturing Change or Addition  
1/28/1987 010Labeling Revision  
3/27/1986 009Control Supplement  
11/27/1985 008Manufacturing Change or Addition  
1/12/1987 007Labeling Revision  
11/27/1985 006Formulation Revision  
12/8/1987 005Labeling Revision  
12/8/1983 003Labeling Revision  
11/18/1983 002Control Supplement  
10/16/1981 000Approval  
 
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