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) 085208
Active Ingredient(s):
HYDROCHLOROTHIAZIDE
Company:
ACTAVIS ELIZABETH
Label History
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 085208
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/23/2002
025
Control Supplement
7/17/2002
024
Control Supplement
11/2/2001
023
Control Supplement
2/21/2001
022
Control Supplement
12/13/1999
021
Labeling
1/18/1996
020
Chemistry
8/2/1995
019
Labeling
8/13/1993
018
Labeling
1/28/1993
017
Labeling
6/19/1992
016
Labeling
8/12/1991
015
Chemistry
12/4/1990
014
Labeling
3/15/1989
012
SBA
11/14/1988
012
Labeling
5/23/1988
011
Labeling
6/17/1988
010
Chemistry
5/21/1987
009
Chemistry
12/13/1985
006
Chemistry
5/24/1982
002
Chemistry
8/20/1981
000
Approval
Therapeutic Equivalents
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