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) 087408
Active Ingredient(s):
HYDROXYZINE HYDROCHLORIDE
Company:
LUITPOLD
Label History
Labels are not available on this site for HYDROXYZINE HYDROCHLORIDE, (ANDA) 087408
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/2/2003
015
Labeling
7/17/2002
014
Manufacturing Revision
9/25/1997
013
Chemistry
2/28/1996
012
Chemistry
12/24/1992
011
Labeling in Effect
4/2/1992
010
Labeling
9/4/1991
009
Labeling
5/22/1991
008
Chemistry
9/13/1991
007
Chemistry
8/27/1981
000
Approval
Therapeutic Equivalents
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