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) 085551
Active Ingredient(s):
HYDROXYZINE HYDROCHLORIDE
Company:
BAXTER HLTHCARE
Label History
Labels are not available on this site for HYDROXYZINE HYDROCHLORIDE, (ANDA) 085551
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/6/2000
036
Control Supplement
7/18/1997
033
Chemistry
7/18/1997
032
Chemistry
8/19/1993
031
Chemistry in Effect
8/6/1991
030
Labeling in Effect
5/21/1991
029
Labeling
4/24/1990
028
Chemistry in Effect
10/12/1989
027
Labeling
5/1/1989
026
Labeling
12/9/1988
024
Labeling
10/17/1988
022
Labeling
10/22/1985
020
Chemistry
3/27/1985
014
Chemistry
1/19/1984
013
Chemistry
9/30/1982
012
Chemistry
8/24/1979
000
Approval
Therapeutic Equivalents
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