Visitor Monitoring Drug History: LEXXEL
 
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: LEXXEL
FDA Application No: (NDA) 020668
Active Ingredient(s): ENALAPRIL MALEATE; FELODIPINE
Company: ASTRAZENECA
 
Label History
 
View the label approved on June 10, 2004 for LEXXEL, (NDA) 020668


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
10/4/2007 013Labeling Revision Letter 
12/23/2004 012Labeling Revision Letter 
6/7/2004 011Labeling Revision Letter
Label 
6/11/2003 009Labeling Revision Letter 
9/18/2001 008Labeling Revision  
2/6/2001 007Control Supplement  
7/18/2000 006Labeling Revision  
8/2/2005 005Labeling Revision Letter
Label 
7/22/1998 004Labeling Revision  
10/28/1998 003Control Supplement Letter
Label
Review 
3/3/1998 002Labeling Revision Review 
7/2/1997 001Manufacturing Change or Addition Review 
12/27/1996 000Approval  
 
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