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) 089383
Active Ingredient(s):
HYDROXYZINE HYDROCHLORIDE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for HYDROXYZINE HYDROCHLORIDE, (ANDA) 089383
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/12/2002
013
Labeling
4/3/2002
012
Control Supplement
6/19/2001
011
Control Supplement
3/5/2002
010
Control Supplement
2/26/2001
009
Control Supplement
5/16/2000
008
Facility Addition
5/16/2000
007
Facility Addition
12/5/1997
006
Chemistry
2/24/1997
005
Chemistry
6/22/1995
004
Chemistry
1/12/1994
003
Chemistry
10/9/1990
002
Chemistry
12/4/1989
001
Labeling
5/19/1986
000
Approval
Therapeutic Equivalents
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