Visitor Monitoring Drug History: CARDIOLITE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: CARDIOLITE
FDA Application No: (NDA) 019785
Active Ingredient(s): TECHNETIUM TC-99M SESTAMIBI KIT
Company: BRISTOL MYERS SQUIBB
 
Label History
 
Labels are not available on this site for CARDIOLITE, (NDA) 019785
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/8/2000 015Control Supplement  
2/11/2000 014Manufacturing Change or Addition  
1/14/2000 013Labeling Revision  
1/22/2002 012Labeling Revision  
6/10/1998 011Control Supplement  
8/8/1997 010Manufacturing Change or Addition  
4/24/1997 009Manufacturing Change or Addition  
9/26/1996 008Manufacturing Change or Addition  
11/8/1996 007Control Supplement  
5/23/1997 006Patient Population Altered  
12/14/1995 005Patient Population Altered  
12/14/1995 004New or Modified Indication  
2/28/1996 003Control Supplement  
9/9/1992 002New or Modified Indication  
1/30/1992 001Manufacturing Change or Addition  
12/21/1990 000Approval  
 
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