DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
LARIAM
FDA Application No:
(NDA) 019591
Active Ingredient(s):
MEFLOQUINE HYDROCHLORIDE
Company:
ROCHE
Label History
View the
label approved on September 8, 2003
for LARIAM, (NDA) 019591
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
8/20/2003
022
Labeling Revision
Letter
Label
10/3/2002
020
Labeling Revision
Label
7/9/2003
019
Labeling Revision
Letter
Label
6/21/2002
018
Control Supplement
1/10/2003
017
Labeling Revision
Letter
Label
3/24/2002
015
Control Supplement
1/10/2003
014
Labeling Revision
Letter
Label
11/10/1999
013
Control Supplement
8/2/1999
012
Labeling Revision
10/20/1998
011
Control Supplement
8/2/1999
010
Labeling Revision
1/22/1996
009
Package Change
6/16/1995
008
Manufacturing Change or Addition
8/6/1997
007
Labeling Revision
11/3/1993
006
Control Supplement
11/2/1993
005
Labeling Revision
10/4/1991
004
Control Supplement
11/23/1992
003
New Dosage Regimen
7/30/1990
002
Control Supplement
2/2/1990
001
Labeling Revision
5/2/1989
000
Approval
Label
Medication Guide
Therapeutic Equivalents
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