DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
AMARYL
FDA Application No:
(NDA) 020496
Active Ingredient(s):
GLIMEPIRIDE
Company:
SANOFI AVENTIS US
Label History
View the
label approved on September 22, 2005
for AMARYL, (NDA) 020496
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
9/19/2005
016
Labeling Revision
Letter
Label
11/28/2005
015
Patient Population Altered
Letter
Label
8/16/2004
013
Labeling Revision
Letter
7/21/2001
011
Manufacturing Change or Addition
12/5/2000
010
Control Supplement
8/29/2000
009
Control Supplement
4/15/2002
007
Labeling Revision
Letter
1/6/2000
006
Manufacturing Change or Addition
9/27/2000
005
Efficacy Supplement with Clinical Data to Support
Review
9/16/1998
004
Package Change
9/16/1998
003
Package Change
2/24/1999
002
New or Modified Indication
Letter
Review
7/28/1997
001
Manufacturing Change or Addition
11/30/1995
000
Approval
Therapeutic Equivalents
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