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) 087068
Active Ingredient(s):
HYDROCHLOROTHIAZIDE
Company:
CLONMEL HLTHCARE
Label History
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 087068
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/7/1999
017
Chemistry
2/11/1999
016
Chemistry
12/30/1998
015
Chemistry
8/3/1995
014
Labeling
8/4/1994
013
Chemistry
11/22/1993
012
Labeling in Effect
8/10/1993
011
Labeling
7/11/1994
010
Chemistry
5/26/1992
009
Labeling
11/9/1990
008
Labeling in Effect
4/20/1990
007
Labeling
11/15/1989
006
Labeling
8/15/1983
005
Chemistry
7/27/1983
004
Chemistry
11/5/1980
000
Approval
Therapeutic Equivalents
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