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) 083965
Active Ingredient(s):
HYDROCHLOROTHIAZIDE
Company:
TG UNITED LABS
Label History
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 083965
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/6/2000
096
Facility Addition
3/13/1996
093
Labeling
8/2/1995
092
Labeling
3/13/1995
091
Labeling
7/15/1993
089
Labeling
11/13/1991
087
Labeling
7/25/1991
086
Labeling
8/3/1990
085
Labeling
8/3/1990
084
Labeling
8/3/1990
083
Labeling
2/12/1990
082
Labeling
4/4/1988
081
Labeling
1/18/1989
080
Chemistry
9/1/1988
078
Chemistry
8/9/1983
071
Chemistry
3/21/1983
070
Chemistry
5/19/1982
069
Chemistry
3/21/1977
000
Approval
Review
Therapeutic Equivalents
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