Visitor Monitoring Drug History: HYDROCHLOROTHIAZIDE
 
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: HYDROCHLOROTHIAZIDE
FDA Application No: (ANDA) 085683
Active Ingredient(s): HYDROCHLOROTHIAZIDE
Company: TG UNITED LABS
 
Label History
 
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 085683
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/6/2000 057Facility Addition  
3/13/1996 054Labeling  
8/2/1995 053Labeling  
3/13/1995 052Labeling  
7/15/1993 050Labeling  
11/13/1991 048Labeling  
7/25/1991 047Labeling  
12/4/1990 046Labeling  
8/3/1990 045Labeling  
1/31/1990 044Labeling  
3/24/1989 043Labeling  
5/2/1989 042Chemistry  
1/23/1989 041Labeling  
3/24/1988 039Chemistry  
6/6/1983 036Chemistry  
8/17/1977 000Approval  
 
Therapeutic Equivalents
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