Visitor Monitoring Drug History: ACEON
 
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: ACEON
FDA Application No: (NDA) 020184
Active Ingredient(s): PERINDOPRIL ERBUMINE
Company: SOLVAY PHARMS
 
Label History
 
View the label approved on August 31, 2005 for ACEON, (NDA) 020184


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
8/23/2005 011New or Modified Indication Letter
Label 
10/29/2003 009Labeling Revision Letter 
11/20/2002 008Manufacturing Change or Addition  
8/14/2002 007Manufacturing Change or Addition  
8/12/1999 006Manufacturing Change or Addition  
8/21/1997 005Manufacturing Change or Addition  
7/21/1997 004Labeling Revision  
1/8/1997 003Labeling Revision Review 
11/14/1996 002Manufacturing Change or Addition  
5/13/1994 001Manufacturing Change or Addition  
12/30/1993 000Approval Other Important Information from FDA 
 
There are no Therapeutic Equivalents
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