Visitor Monitoring Drug History: EDECRIN
 
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: EDECRIN
FDA Application No: (NDA) 016093
Active Ingredient(s): ETHACRYNATE SODIUM
Company: ATON
 
Label History
 
View the label approved on February 11, 2005 for EDECRIN, (NDA) 016093


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
7/20/2005 045Control Supplement  
2/9/2005 044Labeling Revision Letter
Label 
2/3/2004 043Labeling Revision Letter 
6/10/2002 042Manufacturing Change or Addition  
7/19/2001 041Control Supplement  
6/18/2001 040Control Supplement  
2/14/2001 039Control Supplement  
10/19/1999 038Labeling Revision Review 
9/3/1999 037Manufacturing Change or Addition  
11/3/1997 036Labeling Revision  
11/30/1995 035Manufacturing Change or Addition  
3/24/1995 034Labeling Revision  
10/8/1996 033Control Supplement  
8/7/1991 032Manufacturing Change or Addition  
5/30/1989 031Manufacturing Change or Addition  
12/8/1986 030Manufacturing Change or Addition  
3/21/1986 029Labeling Revision  
1/13/1986 028Labeling Revision  
8/27/1985 027Package Change  
10/11/1984 026Package Change  
8/28/1984 025Labeling Revision  
9/20/1983 024Control Supplement  
5/19/1983 023Control Supplement  
7/14/1981 022Package Change  
11/3/1981 021Manufacturing Change or Addition  
5/13/1985 020Practioner Draft Labeling  
8/28/1981 019Formulation Revision  
1/16/1981 018Labeling Revision  
2/19/1981 017Formulation Revision  
1/25/1980 016Labeling Revision  
6/21/1979 015Control Supplement  
8/28/1978 014Control Supplement  
3/10/1978 013Labeling Revision  
1/29/1976 012Control Supplement  
8/28/1978 011Control Supplement  
1/10/1967 000Approval  
 
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