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) 019217
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) 019217
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/1/1999
006
Package Change
1/22/1999
005
Control Supplement
11/18/1998
004
Package Change
12/5/2003
003
Labeling Revision
Letter
3/25/1994
002
Control Supplement
7/13/1984
000
Approval
Therapeutic Equivalents
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