DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HYTRIN
FDA Application No:
(NDA) 019057
Active Ingredient(s):
TERAZOSIN HYDROCHLORIDE
Company:
ABBOTT
Label History
Labels are not available on this site for HYTRIN, (NDA) 019057
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/6/2006
021
Labeling Revision
Letter
12/24/2002
018
Control Supplement
11/15/2002
017
Control Supplement
10/4/2002
016
Control Supplement
1/23/2002
015
Labeling Revision
Letter
Review
8/6/1998
014
Control Supplement
4/16/1998
013
Package Change
8/8/1996
012
Control Supplement
9/18/1996
011
Labeling Revision
7/11/1995
010
Control Supplement
10/6/1995
009
Manufacturing Change or Addition
9/14/1994
008
Labeling Revision
6/17/1994
007
Control Supplement
9/29/1993
006
Labeling Revision
8/20/1993
005
Control Supplement
8/9/1991
004
Control Supplement
8/10/1990
003
Labeling Revision
9/20/1988
002
Control Supplement
7/1/1988
001
Labeling Revision
8/7/1987
000
Approval
Therapeutic Equivalents
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