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) 087871
Active Ingredient(s):
HYDROXYZINE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for HYDROXYZINE HYDROCHLORIDE, (ANDA) 087871
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/10/2000
022
Package Change
2/21/1995
021
Chemistry
11/14/1988
020
Labeling
4/25/1988
015
Chemistry
4/25/1988
014
Chemistry
7/8/1985
008
Chemistry
7/8/1985
005
Chemistry
8/21/1984
004
Chemistry
8/21/1984
002
Chemistry
8/21/1984
001
Chemistry
12/20/1982
000
Approval
Therapeutic Equivalents
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