DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ATARAX
FDA Application No:
(NDA) 010392
Active Ingredient(s):
HYDROXYZINE HYDROCHLORIDE
Company:
PFIZER
Label History
Labels are not available on this site for ATARAX, (NDA) 010392
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/21/2001
041
Labeling Revision
Letter
3/27/2000
040
Package Change
1/16/1998
038
Control Supplement
7/12/1994
037
Manufacturing Change or Addition
1/16/1998
036
Control Supplement
5/20/1985
031
Labeling Revision
5/21/1979
021
Labeling Revision
12/2/1974
008
Distributor
4/12/1956
000
Approval
Therapeutic Equivalents
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