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) 020347
Active Ingredient(s):
TERAZOSIN HYDROCHLORIDE
Company:
ABBOTT
Label History
Labels are not available on this site for HYTRIN, (NDA) 020347
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/6/2006
009
Labeling Revision
Letter
10/4/2002
007
Control Supplement
1/23/2002
006
Labeling Revision
Letter
Review
8/6/1998
005
Control Supplement
4/16/1998
004
Package Change
8/8/1996
003
Control Supplement
9/18/1996
002
Labeling Revision
3/14/1995
001
Control Supplement
12/14/1994
000
Approval
Therapeutic Equivalents
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