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) 088349
Active Ingredient(s):
HYDROXYZINE HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for HYDROXYZINE HYDROCHLORIDE, (ANDA) 088349
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/26/2001
029
Control Supplement
1/30/2002
028
Labeling
4/25/2001
027
Control Supplement
5/27/1998
025
Chemistry
5/27/1998
024
Chemistry
3/23/1998
023
Chemistry
1/29/1993
022
Chemistry
11/19/1990
021
Chemistry
8/7/1991
020
Chemistry
6/29/1990
019
Chemistry
1/14/1992
018
Chemistry
3/28/1989
017
SBA
1/14/1992
017
Chemistry
2/14/1989
016
Labeling
11/21/1988
015
Labeling
1/14/1992
014
Chemistry
9/27/1988
013
SBA
1/14/1992
013
Chemistry
12/16/1988
012
Chemistry
12/16/1988
011
Chemistry
2/12/1986
007
Chemistry
5/21/1985
005
Chemistry
5/21/1985
004
Chemistry
2/15/1985
003
Chemistry
2/15/1985
002
Chemistry
9/18/1984
001
Chemistry
9/15/1983
000
Approval
Therapeutic Equivalents
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