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) 083232
Active Ingredient(s):
HYDROCHLOROTHIAZIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 083232
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/13/1995
057
Labeling
9/12/1995
056
Labeling
8/3/1993
055
Labeling
10/6/1992
054
Labeling
11/19/1990
053
Chemistry
7/12/1989
051
Labeling
6/29/1990
050
Chemistry
5/4/1989
049
Labeling
9/20/1988
047
Labeling
9/20/1988
046
Chemistry
9/20/1988
045
Chemistry
2/19/1988
043
Chemistry
2/19/1988
042
Chemistry
12/16/1987
041
Chemistry
12/16/1987
040
Chemistry
12/16/1987
039
Chemistry
6/3/1985
034
Chemistry
6/3/1985
033
Chemistry
1/22/1985
032
Chemistry
1/13/1984
031
Chemistry
5/23/1983
029
Chemistry
5/23/1983
028
Chemistry
8/16/1982
026
Chemistry
1/24/1975
000
Approval
Review
Therapeutic Equivalents
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