DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ZINC CHLORIDE IN PLASTIC CONTAINER
FDA Application No:
(NDA) 018959
Active Ingredient(s):
ZINC CHLORIDE
Company:
HOSPIRA
Label History
Labels are not available on this site for ZINC CHLORIDE IN PLASTIC CONTAINER, (NDA) 018959
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/14/2003
011
Labeling Revision
Letter
2/16/2001
010
Package Change
8/31/1999
009
Package Change
2/14/2003
008
Labeling Revision
Letter
1/22/1999
007
Control Supplement
8/29/1996
006
Control Supplement
1/17/1997
005
Package Change
6/29/1987
003
Package Change
9/9/1986
001
Control Supplement
6/26/1986
000
Approval
There are no Therapeutic Equivalents
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