DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HYDROCHLOROTHIAZIDE
FDA Application No:
(ANDA) 084912
Active Ingredient(s):
HYDROCHLOROTHIAZIDE
Company:
SANDOZ
Label History
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 084912
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
069
Chemistry
12/1/1998
068
Chemistry
1/12/1998
067
Chemistry
7/27/1995
066
Labeling
1/24/1994
065
Chemistry
3/30/1994
064
Labeling
8/11/1992
063
Labeling
11/9/1989
062
Labeling in Effect
11/21/1989
061
Labeling in Effect
8/23/1989
060
Labeling
5/27/1988
059
Labeling
8/21/1990
058
Chemistry
8/21/1990
057
Chemistry
6/3/1987
056
Chemistry
6/3/1987
055
Chemistry
6/3/1987
054
Chemistry
6/3/1987
053
Chemistry
4/12/1985
050
Chemistry
4/23/1985
049
Chemistry
8/17/1983
046
Chemistry
8/17/1983
045
Chemistry
8/9/1982
043
Chemistry
7/8/1982
041
Chemistry
7/8/1982
039
Chemistry
7/8/1982
037
Chemistry
7/8/1982
036
Chemistry
12/17/1976
000
Approval
Therapeutic Equivalents
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