Visitor Monitoring Drug Details: CARDIOTEC
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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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 NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
CARDIOTEC TECHNETIUM TC-99M TEBOROXIME KITN/AINJECTABLE; INJECTION Discontinued No None


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