DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TENORMIN
FDA Application No:
(NDA) 019058
Active Ingredient(s):
ATENOLOL
Company:
ASTRAZENECA
Label History
Labels are not available on this site for TENORMIN, (NDA) 019058
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/9/2005
017
Labeling Revision
Letter
11/6/2003
016
Labeling Revision
Letter
1/22/2003
015
Labeling Revision
Letter
10/19/2001
014
Manufacturing Change or Addition
7/21/1999
013
Labeling Revision
Review
4/4/2000
012
Labeling Revision
Review
2/5/1998
011
Manufacturing Change or Addition
3/20/1996
010
Labeling Revision
5/4/1994
008
Labeling Revision
4/29/1993
007
Labeling Revision
8/5/1992
006
Labeling Revision
8/5/1992
005
Labeling Revision
9/18/1991
004
Labeling Revision
4/17/1991
003
Labeling Revision
4/5/1991
002
Labeling Revision
4/5/1991
001
Labeling Revision
9/13/1989
000
Approval
There are no Therapeutic Equivalents
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