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) 088348
Active Ingredient(s):
HYDROXYZINE HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for HYDROXYZINE HYDROCHLORIDE, (ANDA) 088348
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/4/2002
030
Facility Addition
11/26/2001
029
Control Supplement
1/30/2002
028
Labeling
4/25/2001
027
Control Supplement
8/17/1998
025
Chemistry
3/23/1998
024
Chemistry
12/16/1997
023
Chemistry
1/29/1993
022
Chemistry
11/19/1990
021
Chemistry
8/7/1991
020
Chemistry
6/29/1990
019
Chemistry
2/14/1989
016
Labeling
12/23/1988
015
SBA
11/21/1988
015
Labeling
12/30/1988
013
SBA
1/12/1989
012
Chemistry
1/12/1989
011
Chemistry
2/12/1986
007
Chemistry
5/21/1985
006
Chemistry
5/21/1985
005
Chemistry
5/21/1985
003
Chemistry
5/21/1985
002
Chemistry
10/3/1984
001
Chemistry
9/15/1983
000
Approval
Therapeutic Equivalents
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