DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
K+10
FDA Application No:
(ANDA) 070999
Active Ingredient(s):
POTASSIUM CHLORIDE
Company:
ALRA
Label History
Labels are not available on this site for K10, (ANDA) 070999
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/23/1995
007
Chemistry
6/23/1995
006
Chemistry
7/22/1994
005
Chemistry
11/16/1992
004
SBA
10/22/1987
000
Approval
Therapeutic Equivalents
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