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:
(ANDA) 083345
Active Ingredient(s):
POTASSIUM CHLORIDE
Company:
HOSPIRA
Label History
Labels are not available on this site for POTASSIUM CHLORIDE, (ANDA) 083345
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/11/2002
026
Expiration Date Change
8/12/1994
023
Labeling
6/2/1992
022
Labeling in Effect
11/7/1991
021
Labeling
8/23/1989
020
Labeling
8/29/1985
019
Chemistry
11/20/1984
018
Chemistry
2/13/1974
000
Approval
There are no Therapeutic Equivalents
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