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) 088350
Active Ingredient(s):
HYDROXYZINE HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for HYDROXYZINE HYDROCHLORIDE, (ANDA) 088350
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/26/2001
024
Control Supplement
1/30/2002
023
Labeling
3/23/1998
018
Chemistry
1/29/1993
017
Chemistry
11/19/1990
016
Chemistry
8/7/1991
015
Chemistry
6/29/1990
014
Chemistry
1/30/1992
013
Chemistry
1/30/1992
012
Chemistry
2/14/1989
011
Labeling
12/30/1988
010
SBA
11/21/1988
010
Labeling
1/30/1992
009
Chemistry
1/30/1992
008
Chemistry
2/12/1986
004
Chemistry
2/15/1985
003
Chemistry
2/15/1985
002
Chemistry
9/20/1984
001
Chemistry
9/15/1983
000
Approval
Therapeutic Equivalents
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