Visitor Monitoring Drug History: QUINIDEX
 
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: QUINIDEX
FDA Application No: (NDA) 012796
Active Ingredient(s): QUINIDINE SULFATE
Company: WYETH PHARMS INC
 
Label History
 
View the label approved on May 14, 2003 for QUINIDEX, (NDA) 012796


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
8/16/2001 049Labeling Revision Letter
Label 
6/24/1998 048Labeling Revision  
1/13/1998 047Manufacturing Change or Addition  
11/9/1995 046Labeling Revision  
5/2/1988 044Package Change  
2/25/1988 043Package Change  
12/1/1987 042Labeling Revision  
6/12/1987 041Labeling Revision  
4/22/1986 040Package Change  
8/12/1986 039Formulation Revision  
8/2/1988 038Labeling Revision  
7/22/1985 037Package Change  
3/7/1985 036Labeling Revision  
7/22/1985 035Control Supplement  
6/7/1984 034Package Change  
5/31/1984 033Formulation Revision  
1/4/1984 032Formulation Revision  
1/4/1984 031Package Change  
1/4/1984 030Package Change  
10/26/1982 028Package Change  
3/8/1982 027Formulation Revision  
12/4/1981 023Package Change  
12/4/1981 022Manufacturing Change or Addition  
2/22/1984 021Formulation Revision  
12/19/1980 020Package Change  
12/19/1980 019Control Supplement  
6/21/1979 018Labeling Revision  
12/19/1980 017Control Supplement  
11/7/1978 016Control Supplement  
7/20/1978 015Formulation Revision  
10/11/1977 014Control Supplement  
10/11/1977 013Control Supplement  
10/11/1977 012Formulation Revision  
10/11/1977 011General Efficacy (MarkIV)  
10/11/1977 010Control Supplement  
2/21/1962 000Approval  
 
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