DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HYDROXYZINE HYDROCHLORIDE
FDA Application No:
(ANDA) 085779
Active Ingredient(s):
HYDROXYZINE HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for HYDROXYZINE HYDROCHLORIDE, (ANDA) 085779
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/19/1999
092
Microbiology
2/2/1999
091
Microbiology
12/4/1996
090
Microbiology
5/23/1991
089
Labeling
2/11/1991
088
Labeling in Effect
11/21/1990
087
Chemistry in Effect
12/4/1989
086
Labeling
12/4/1989
085
Labeling
8/3/1989
084
Labeling
9/21/1988
082
SBA
8/3/1988
081
Chemistry
8/3/1988
080
Chemistry
5/28/1986
076
Chemistry
12/30/1983
075
Chemistry
2/8/1982
073
Chemistry
10/5/1979
000
Approval
Therapeutic Equivalents
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