Visitor Monitoring Drug History: ESIDRIX
 
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: ESIDRIX
FDA Application No: (NDA) 011793
Active Ingredient(s): HYDROCHLOROTHIAZIDE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for ESIDRIX, (NDA) 011793
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/29/2002 070Manufacturing Change or Addition  
4/28/1999 069Package Change  
7/21/1997 068Control Supplement  
6/20/1996 067Control Supplement  
2/27/1996 066Manufacturing Change or Addition  
7/31/1995 065Control Supplement  
12/1/1994 064Labeling Revision  
3/10/1993 062Labeling Revision  
6/5/1991 061Labeling Revision  
7/30/1992 060Labeling Revision  
11/9/1990 059Formulation Revision  
9/23/1988 058Labeling Revision  
10/2/1986 057Labeling Revision  
3/19/1985 056Control Supplement  
12/8/1982 055Control Supplement  
8/23/1982 054Package Change  
6/4/1982 053Package Change  
4/10/1986 051Practioner Draft Labeling  
2/2/1981 050Package Change  
1/30/1980 049Package Change  
1/17/1980 048Package Change  
6/29/1979 047Package Change  
6/29/1979 046Package Change  
6/29/1979 045Package Change  
1/10/1978 044Formulation Revision  
6/16/1977 043Control Supplement  
4/12/1977 042Package Change  
2/22/1978 041Labeling Revision  
2/9/1977 040Labeling Revision  
8/31/1976 039Control Supplement  
2/9/1977 038Labeling Revision  
8/18/1976 037Formulation Revision  
5/20/1976 036Formulation Revision  
3/24/1976 035Manufacturing Change or Addition  
10/9/1975 034Labeling Revision  
3/24/1976 033Control Supplement  
7/2/1975 032Control Supplement  
4/2/1975 030Package Change  
4/2/1975 029Package Change  
2/12/1959 000Approval  
 
Therapeutic Equivalents
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