Visitor Monitoring Drug History: HYDROCHLOROTHIAZIDE
 
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Label and Approval History

Drug Name: HYDROCHLOROTHIAZIDE
FDA Application No: (ANDA) 085054
Active Ingredient(s): HYDROCHLOROTHIAZIDE
Company: ACTAVIS ELIZABETH
 
Label History
 
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 085054
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/23/2002 026Control Supplement  
7/17/2002 025Control Supplement  
11/2/2001 024Control Supplement  
12/13/1999 023Labeling  
8/26/1999 022Chemistry  
1/18/1996 021Chemistry  
8/2/1995 020Labeling  
8/13/1993 019Labeling  
1/28/1993 018Labeling  
6/19/1992 017Labeling  
5/7/1993 016Chemistry  
8/23/1990 015SBA  
5/7/1991 015Labeling  
3/26/1991 014Chemistry  
3/26/1991 013Chemistry  
3/26/1991 012Chemistry  
3/26/1991 011Chemistry  
11/14/1988 010Labeling  
5/23/1988 009Labeling  
1/17/1986 006Chemistry  
8/5/1982 002Chemistry  
8/20/1981 000Approval  
 
Therapeutic Equivalents
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