Visitor Monitoring Drug History: CARDIOTEC
 
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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 DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/17/2003 002Labeling Revision Letter 
1/9/2002 001Manufacturing Change or Addition  
12/19/1990 000Approval  
 
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