Visitor Monitoring Drug History: CAPOZIDE 25/25
 
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Label and Approval History

Drug Name: CAPOZIDE 25/25
FDA Application No: (NDA) 018709
Active Ingredient(s): CAPTOPRIL; HYDROCHLOROTHIAZIDE
Company: APOTHECON
 
Label History
 
Labels are not available on this site for CAPOZIDE 2525, (NDA) 018709
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/16/2006 033Labeling Revision Letter 
5/20/1997 031Control Supplement  
6/3/1998 030Labeling Revision  
6/26/1996 029Manufacturing Change or Addition  
3/4/1996 028Control Supplement  
7/31/1996 027Labeling Revision  
7/31/1996 026Labeling Revision  
10/6/1995 025Manufacturing Change or Addition  
5/12/1993 024Package Change  
10/15/1992 023Labeling Revision  
6/25/1992 022Labeling Revision  
7/25/1994 021Labeling Revision  
3/5/1992 020Package Change  
12/10/1991 019Manufacturing Change or Addition  
9/5/1990 018Package Change  
3/21/1991 017Labeling Revision  
9/27/1990 016Labeling Revision  
5/3/1989 015Labeling Revision  
10/19/1989 014Labeling Revision  
6/22/1988 012Labeling Revision  
10/6/1987 011Control Supplement  
1/6/1987 010Package Change  
10/24/1991 009New or Modified Indication  
1/17/1986 008Labeling Revision  
8/2/1985 007Labeling Revision  
7/15/1985 006Package Change  
11/10/1986 005Control Supplement  
7/3/1985 004Package Change  
8/1/1985 003Package Change  
2/7/1985 002Package Change  
11/20/1984 001Control Supplement  
10/12/1984 000Approval  
 
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