Visitor Monitoring Drug History: TENUATE DOSPAN
 
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: TENUATE DOSPAN
FDA Application No: (NDA) 012546
Active Ingredient(s): DIETHYLPROPION HYDROCHLORIDE
Company: WATSON PHARMS
 
Label History
 
View the label approved on September 7, 2004 for TENUATE DOSPAN, (NDA) 012546


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
9/3/2004 032Labeling Revision Letter
Label 
4/16/2002 031Formulation Revision  
2/9/2000 030Control Supplement  
5/6/1999 029Labeling Revision  
2/2/1998 027Labeling Revision  
2/2/1998 025Labeling Revision  
7/21/1988 024Package Change  
10/3/1986 022Control Supplement  
8/22/1985 021Package Change  
12/23/1983 020Manufacturing Change or Addition  
6/8/1983 019Control Supplement  
12/6/1982 018Labeling Revision  
6/17/1988 017Labeling Revision  
10/18/1982 016Package Change  
11/6/1979 015Control Supplement  
4/27/1978 014Package Change  
9/27/1976 011Package Change  
6/24/1975 009Control Supplement  
11/17/1960 000Approval  
 
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