DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CARDIOTEC
FDA Application No:
(NDA) 019928
Active Ingredient(s):
TECHNETIUM TC-99M TEBOROXIME KIT
Company:
BRACCO
Label History
Labels are not available on this site for CARDIOTEC, (NDA) 019928
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/17/2003
002
Labeling Revision
Letter
1/9/2002
001
Manufacturing Change or Addition
12/19/1990
000
Approval
There are no Therapeutic Equivalents
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