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) 085672
Active Ingredient(s):
HYDROCHLOROTHIAZIDE
Company:
ABC HOLDING
Label History
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 085672
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/13/1996
054
Labeling
8/2/1995
053
Labeling
3/13/1995
052
Labeling
7/15/1993
049
Labeling
11/13/1991
047
Labeling
7/25/1991
046
Labeling
8/3/1990
045
Labeling
8/3/1990
044
Labeling
1/31/1990
043
Labeling
10/31/1988
042
Labeling
3/24/1988
040
Chemistry
6/6/1983
036
Chemistry
2/24/1983
035
Chemistry
6/2/1977
000
Approval
Therapeutic Equivalents
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