Visitor Monitoring Drug History: HYDROCHLOROTHIAZIDE
 
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Label and Approval History

Drug Name: HYDROCHLOROTHIAZIDE
FDA Application No: (ANDA) 085022
Active Ingredient(s): HYDROCHLOROTHIAZIDE
Company: IVAX PHARMS
 
Label History
 
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 085022
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/29/2002 033Facility Addition  
3/12/2002 032Facility Addition  
11/15/2002 031Package Change  
8/22/2002 029Control Supplement  
1/28/2000 028Facility Addition  
4/30/1999 026Chemistry  
4/30/1999 025Chemistry  
4/30/1999 024Chemistry  
12/9/1998 023Chemistry  
5/13/1998 022Chemistry  
1/13/1998 021Chemistry  
5/30/1997 020Chemistry  
2/28/1997 019Chemistry  
8/17/1995 018Labeling  
3/12/1993 017Labeling  
10/6/1995 016Chemistry in Effect  
6/7/1993 015Chemistry  
6/7/1993 014Labeling  
2/25/1993 013Chemistry in Effect  
11/3/1989 012Chemistry  
11/3/1989 011Chemistry  
11/3/1989 010Chemistry  
8/24/1988 001SBA  
9/1/1977 000Approval  
 
Therapeutic Equivalents
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