DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TRAVASOL 3.5% W/ ELECTROLYTES
FDA Application No:
(NDA) 017493
Active Ingredient(s):
AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Company:
BAXTER HLTHCARE
Label History
Labels are not available on this site for TRAVASOL 3.5 W ELECTROLYTES, (NDA) 017493
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/17/2003
067
Control Supplement
Letter
4/30/2003
066
Labeling Revision
Letter
1/3/2003
065
Labeling Revision
Letter
3/31/1999
064
Control Supplement
4/5/1999
063
Control Supplement
2/18/1994
062
Control Supplement
5/19/1994
061
Manufacturing Change or Addition
9/30/1994
060
Control Supplement
8/24/1992
059
Manufacturing Change or Addition
4/3/1991
058
Control Supplement
9/14/1992
057
Control Supplement
3/12/1993
056
Labeling Revision
3/26/1991
055
Control Supplement
5/4/1990
054
Control Supplement
3/12/1993
053
Labeling Revision
4/30/1997
052
Package Change
7/26/1989
051
Control Supplement
12/30/1987
049
Package Change
11/18/1987
048
Labeling Revision
7/25/1987
047
Package Change
9/20/1985
046
Labeling Revision
2/28/1984
045
Control Supplement
1/19/1983
043
Labeling Revision
1/19/1983
042
Control Supplement
1/24/1985
041
Control Supplement
7/21/1982
039
Manufacturing Change or Addition
3/8/1982
038
Control Supplement
4/6/1982
037
Labeling Revision
4/6/1982
036
Control Supplement
2/16/1982
035
Control Supplement
12/16/1981
034
Control Supplement
10/15/1982
033
Labeling Revision
10/15/1982
032
Control Supplement
6/29/1981
030
Control Supplement
6/17/1981
029
Labeling Revision
6/17/1981
028
Formulation Revision
7/31/1980
025
Control Supplement
6/3/1980
024
Control Supplement
6/4/1979
023
Control Supplement
4/27/1979
021
Labeling Revision
11/28/1979
020
Labeling Revision
11/28/1979
019
Control Supplement
7/28/1978
018
Control Supplement
7/28/1978
017
Labeling Revision
8/29/1978
016
Control Supplement
12/13/1977
015
Labeling Revision
8/18/1977
014
Control Supplement
7/12/1977
013
Labeling Revision
7/12/1977
012
Control Supplement
7/22/1977
011
Manufacturing Change or Addition
5/10/1979
010
Control Supplement
2/7/1977
009
Control Supplement
4/1/1977
008
Control Supplement
4/1/1977
007
Labeling Revision
12/7/1977
006
Labeling Revision
8/24/1976
005
Control Supplement
6/28/1976
004
Control Supplement
9/8/1976
003
Labeling Revision
7/19/1976
001
Control Supplement
3/24/1976
000
Approval
There are no Therapeutic Equivalents
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