Visitor Monitoring Drug History: DEXEDRINE
 
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: DEXEDRINE
FDA Application No: (NDA) 017078
Active Ingredient(s): DEXTROAMPHETAMINE SULFATE
Company: SMITHKLINE BEECHAM
 
Label History
 
View the label approved on May 7, 2007 for DEXEDRINE, (NDA) 017078


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
5/1/2007 042Labeling Revision Letter
Label 
8/10/2006 040Labeling Revision Letter
Label 
10/20/2000 038Control Supplement  
4/13/2000 037Manufacturing Change or Addition  
10/7/1999 036Formulation Revision  
10/7/1999 035Manufacturing Change or Addition  
11/3/1999 034Labeling Revision  
12/3/1998 033Manufacturing Change or Addition  
6/12/1998 032Control Supplement  
4/6/1998 031Manufacturing Change or Addition  
4/6/1998 030Formulation Revision  
7/9/1997 027Labeling Revision  
9/12/1994 025Labeling Revision  
7/21/1993 022Labeling Revision  
12/16/1987 021Labeling Revision  
12/2/1987 020Labeling Revision  
8/25/1982 019Labeling Revision  
8/25/1982 018Labeling Revision  
2/22/1983 017Labeling Revision  
10/6/1980 016Labeling Revision  
9/19/1980 015Labeling Revision  
8/29/1980 014Labeling Revision  
8/29/1980 013Labeling Revision  
8/29/1980 012Labeling Revision  
4/16/1980 011Labeling Revision  
8/30/1979 009Labeling Revision  
6/27/1979 008Labeling Revision  
6/6/1979 007Labeling Revision  
3/30/1979 005Labeling Revision  
3/30/1979 003Labeling Revision  
8/2/1976 000Approval Other Important Information from FDA 
 
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