DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BACTERIOSTATIC SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 018800
Active Ingredient(s):
SODIUM CHLORIDE
Company:
HOSPIRA
Label History
Labels are not available on this site for BACTERIOSTATIC SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (NDA) 018800
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/19/2003
014
Labeling Revision
Letter
9/30/1997
012
Control Supplement
5/16/2003
011
Labeling Revision
8/29/1996
010
Control Supplement
10/21/1988
007
Control Supplement
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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