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) 087329
Active Ingredient(s):
HYDROXYZINE HYDROCHLORIDE
Company:
ABRAXIS PHARM
Label History
Labels are not available on this site for HYDROXYZINE HYDROCHLORIDE, (ANDA) 087329
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/5/2002
014
Facility Addition
6/24/1996
012
Chemistry
7/5/1996
010
Chemistry
6/23/1993
009
Labeling in Effect
9/23/1994
008
Chemistry in Effect
3/20/1990
007
Labeling
12/13/1984
006
Chemistry
10/2/1984
005
Chemistry
10/2/1984
004
Chemistry
10/13/1982
001
Chemistry
8/11/1981
000
Approval
Therapeutic Equivalents
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