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) 016092
Active Ingredient(s): ETHACRYNIC ACID
Company: ATON
 
Label History
 
View the label approved on February 11, 2005 for EDECRIN, (NDA) 016092


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
2/9/2005 042Labeling Revision Letter
Label 
2/3/2004 039Labeling Revision Letter 
8/14/1998 038Control Supplement  
10/19/1999 037Labeling Revision Review 
11/3/1997 036Labeling Revision  
6/24/1996 035Control Supplement  
3/24/1995 034Labeling Revision  
9/26/1994 033Manufacturing Change or Addition  
8/7/1991 032Manufacturing Change or Addition  
9/6/1988 031Manufacturing Change or Addition  
8/15/1988 030Control Supplement  
3/21/1986 029Labeling Revision  
1/13/1986 028Labeling Revision  
8/28/1984 027Labeling Revision  
9/20/1983 026Control Supplement  
5/19/1983 025Control Supplement  
6/17/1981 024Package Change  
5/13/1985 023Practioner Draft Labeling  
9/4/1981 022Formulation Revision  
1/16/1981 021Labeling Revision  
2/19/1981 020Formulation Revision  
11/14/1980 019Package Change  
1/22/1981 018Formulation Revision  
1/25/1980 017Labeling Revision  
11/29/1979 016Labeling Revision  
6/21/1979 015Control Supplement  
3/9/1979 014Control Supplement  
2/22/1978 012Package Change  
3/21/1977 011Control Supplement  
2/9/1976 010Control Supplement  
1/10/1967 000Approval  
 
There are no Therapeutic Equivalents
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