DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
POTASSIUM CHLORIDE
FDA Application No:
(NDA) 018279
Active Ingredient(s):
POTASSIUM CHLORIDE
Company:
ABBOTT
Label History
Labels are not available on this site for POTASSIUM CHLORIDE, (NDA) 018279
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/14/2004
027
Labeling Revision
Letter
12/24/2002
025
Control Supplement
10/2/2002
024
Control Supplement
4/16/1998
023
Package Change
10/29/1997
022
Control Supplement
11/21/1996
021
Control Supplement
1/27/1993
020
Formulation Revision
3/26/1990
019
Package Change
11/2/1989
017
Package Change
8/1/1988
016
Labeling Revision
8/1/1988
015
Control Supplement
6/12/1987
014
Control Supplement
6/17/1986
012
Control Supplement
10/7/1986
011
Formulation Revision
1/14/1986
010
Formulation Revision
3/25/1985
009
Expiration Date Change
8/13/1984
008
Labeling Revision
8/1/1984
007
Control Supplement
7/2/1982
006
Formulation Revision
11/10/1982
005
Labeling Revision
4/29/1981
004
Manufacturing Change or Addition
1/16/1981
003
Manufacturing Change or Addition
2/3/1981
002
Manufacturing Change or Addition
2/4/1981
001
Package Change
6/9/1980
000
Approval
There are no Therapeutic Equivalents
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