DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CARDIOTEC
FDA Application No:
(NDA) 019928
Active Ingredient(s):
TECHNETIUM TC-99M TEBOROXIME KIT
Company:
BRACCO
Original Approval or Tentative Approval Date:
December 19, 1990
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
There are no Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
CARDIOTEC
TECHNETIUM TC-99M TEBOROXIME KIT
N/A
INJECTABLE; INJECTION
Discontinued
No
None
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