Drug Details: CARDIOTEC

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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	Labels are not available
Approval History, Letters, Reviews and Related Documents

You can see the products in the same application. The table can be sorted by clicking the header columns.

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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