DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 018803
Active Ingredient(s):
SODIUM CHLORIDE
Company:
HOSPIRA
Label History
Labels are not available on this site for SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (NDA) 018803
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/16/2001
014
Package Change
8/31/1999
013
Package Change
9/12/2001
012
Labeling Revision
8/29/1996
011
Control Supplement
1/17/1997
010
Control Supplement
3/24/1988
008
Labeling Revision
2/10/1989
007
Labeling Revision
10/22/1984
006
Control Supplement
3/15/1985
005
Control Supplement
2/25/1986
004
Control Supplement
1/17/1984
003
Control Supplement
6/14/1984
002
Package Change
1/25/1984
001
Control Supplement
10/29/1982
000
Approval
Therapeutic Equivalents
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