DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 017670
Active Ingredient(s):
SODIUM CHLORIDE
Company:
HOSPIRA
Label History
Labels are not available on this site for SODIUM CHLORIDE 0.45 IN PLASTIC CONTAINER, (NDA) 017670
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/7/2004
043
Labeling Revision
Letter
2/4/1998
042
Package Change
8/27/1996
041
Control Supplement
6/30/1992
039
Control Supplement
8/24/1993
038
Package Change
11/25/1988
037
Control Supplement
10/29/1985
036
Control Supplement
1/18/1986
034
Control Supplement
10/22/1984
033
Control Supplement
8/25/1984
031
Control Supplement
2/25/1986
030
Control Supplement
3/15/1984
029
Package Change
3/1/1984
028
Control Supplement
6/10/1982
027
Package Change
11/6/1981
026
Control Supplement
8/31/1982
025
Practioner Draft Labeling
10/21/1980
024
Labeling Revision
6/6/1980
023
Control Supplement
6/6/1980
021
Control Supplement
5/23/1980
020
Control Supplement
5/28/1980
019
Control Supplement
5/5/1980
018
Labeling Revision
7/21/1981
017
Control Supplement
3/20/1980
016
Control Supplement
2/12/1980
015
Control Supplement
10/4/1979
012
Control Supplement
7/31/1979
011
Package Change
7/18/1979
010
Control Supplement
1/5/1979
009
Control Supplement
4/30/1979
008
Control Supplement
6/26/1978
007
Control Supplement
4/26/1977
006
Control Supplement
7/21/1977
005
Manufacturing Change or Addition
4/20/1976
004
Labeling Revision
1/30/1976
003
Labeling Revision
10/7/1975
002
Control Supplement
1/19/1976
001
Control Supplement
3/10/1975
000
Approval
Therapeutic Equivalents
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