DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
QUESTRAN LIGHT
FDA Application No:
(NDA) 019669
Active Ingredient(s):
CHOLESTYRAMINE
Company:
BRISTOL MYERS
Label History
Labels are not available on this site for QUESTRAN LIGHT, (NDA) 019669
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/20/2000
024
Labeling Revision
10/29/1997
023
Formulation Revision
8/22/1997
022
Labeling Revision
12/12/1994
019
Labeling Revision
9/22/1995
018
Labeling Revision
9/22/1995
017
Labeling Revision
1/7/1993
016
Control Supplement
8/11/1992
015
Labeling Revision
9/22/1992
014
Control Supplement
9/10/1991
012
Labeling Revision
3/12/1991
009
Control Supplement
2/2/1990
008
Manufacturing Change or Addition
11/27/1989
007
Labeling Revision
2/21/1989
003
Manufacturing Change or Addition
2/21/1989
002
Control Supplement
2/21/1989
001
Manufacturing Change or Addition
12/5/1988
000
Approval
Therapeutic Equivalents
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