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) 087565
Active Ingredient(s):
HYDROCHLOROTHIAZIDE
Company:
SANDOZ
Label History
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 087565
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
025
Chemistry
12/1/1998
024
Chemistry
1/12/1998
023
Chemistry
7/27/1995
022
Labeling
1/24/1994
021
Chemistry
3/30/1994
020
Labeling
8/11/1992
019
Labeling
10/31/1991
018
Chemistry
3/29/1990
017
SBA
10/31/1991
017
Chemistry
11/7/1989
016
Labeling
9/2/1988
015
Chemistry
4/15/1986
012
Chemistry
4/15/1986
011
Chemistry
4/15/1986
010
Chemistry
10/8/1985
008
Chemistry
6/6/1983
007
Chemistry
6/6/1983
006
Chemistry
11/19/1982
005
Chemistry
2/10/1983
004
Chemistry
8/12/1982
003
Chemistry
3/9/1982
000
Approval
Therapeutic Equivalents
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