DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
VEXOL
FDA Application No:
(NDA) 020474
Active Ingredient(s):
RIMEXOLONE
Company:
ALCON
Label History
View the
label approved on October 22, 2007
for VEXOL, (NDA) 020474
To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/6/2006
023
Supplement
10/18/2007
019
Labeling Revision
Letter
Label
4/17/2003
016
Labeling Revision
Letter
Label
3/16/2001
015
Control Supplement
9/18/2000
014
Formulation Revision
2/18/2000
013
Manufacturing Change or Addition
8/17/1999
012
Control Supplement
4/7/1999
011
Manufacturing Change or Addition
2/5/1999
010
Manufacturing Change or Addition
3/11/1999
009
Control Supplement
1/22/1999
008
Control Supplement
9/11/1998
007
Labeling Revision
11/9/1999
006
Package Change
3/26/1999
005
Manufacturing Change or Addition
5/1/1998
004
Manufacturing Change or Addition
3/20/1998
003
Control Supplement
8/14/1996
002
Labeling Revision
5/10/1995
001
Expiration Date Change
12/30/1994
000
Approval
There are no Therapeutic Equivalents
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