Visitor Monitoring Drug History: ZESTORETIC
 
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: ZESTORETIC
FDA Application No: (NDA) 019888
Active Ingredient(s): HYDROCHLOROTHIAZIDE; LISINOPRIL
Company: ASTRAZENECA
 
Label History
 
Labels are not available on this site for ZESTORETIC, (NDA) 019888
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/4/2007 044Labeling Revision Letter 
7/16/2007 043Labeling Revision Letter 
6/16/2006 041Labeling Revision Letter 
5/24/2005 040Labeling Revision Letter 
4/17/2003 035Labeling Revision Letter 
12/18/2001 034Labeling Revision  
12/19/2000 033Manufacturing Change or Addition  
12/15/2000 032Manufacturing Change or Addition  
7/27/2000 031Manufacturing Change or Addition  
11/18/1999 030Control Supplement  
5/8/1998 029Labeling Revision  
1/14/1997 028Manufacturing Change or Addition  
10/11/1996 027Package Change  
1/5/1996 026Labeling Revision  
12/14/1995 025Manufacturing Change or Addition  
1/5/1996 024Labeling Revision  
7/11/1995 023Manufacturing Change or Addition  
10/26/1995 022Control Supplement  
3/31/1995 021Labeling Revision  
6/13/1995 020Labeling Revision Review 
9/15/1994 019Labeling Revision  
8/5/1994 018Labeling Revision  
8/5/1994 017Labeling Revision  
12/9/1993 016Labeling Revision  
6/13/1995 015Labeling Revision  
9/23/1993 014Labeling Revision  
8/5/1994 013Labeling Revision  
3/31/1993 012Labeling Revision Review 
11/18/1993 011New Dosage Regimen  
11/18/1992 010Manufacturing Change or Addition  
6/25/1992 009Labeling Revision  
12/11/1991 008Manufacturing Change or Addition  
4/11/1991 007Labeling Revision  
4/8/1991 006Control Supplement  
2/21/1991 005Labeling Revision  
12/21/1990 004Manufacturing Change or Addition  
11/8/1990 003Labeling Revision  
9/20/1990 002Formulation Revision  
10/13/1989 001Control Supplement  
7/20/1989 000Approval  
 
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