DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
INDIUM IN-111 OXYQUINOLINE
FDA Application No:
(NDA) 019044
Active Ingredient(s):
INDIUM IN-111 OXYQUINOLINE
Company:
GE HEALTHCARE
Label History
Labels are not available on this site for INDIUM IN111 OXYQUINOLINE, (NDA) 019044
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/19/2002
018
Labeling Revision
Letter
8/30/1999
017
Formulation Revision
8/2/2000
016
Control Supplement
10/16/1997
015
Labeling Revision
8/11/1995
013
Control Supplement
1/13/1995
012
Control Supplement
8/11/1995
011
Manufacturing Change or Addition
8/11/1995
010
Control Supplement
8/27/1990
009
Control Supplement
8/8/1990
008
Control Supplement
8/8/1990
006
Control Supplement
4/11/1989
005
Labeling Revision
6/8/1987
003
Manufacturing Change or Addition
12/12/1989
002
Control Supplement
12/24/1985
000
Approval
There are no Therapeutic Equivalents
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