Visitor Monitoring Drug History: TECHNELITE
 
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: TECHNELITE
FDA Application No: (NDA) 017771
Active Ingredient(s): TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR
Company: BRISTOL MYERS SQUIBB
 
Label History
 
Labels are not available on this site for TECHNELITE, (NDA) 017771
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/5/2001 022Control Supplement  
12/6/2000 021Manufacturing Change or Addition  
2/29/2000 020Manufacturing Change or Addition  
8/11/2000 019Labeling Revision  
2/4/1998 018Manufacturing Change or Addition  
12/15/1997 017Manufacturing Change or Addition  
11/5/1997 016Manufacturing Change or Addition  
4/5/1996 015Control Supplement  
1/24/1996 014Control Supplement  
1/11/1996 013Control Supplement  
5/23/1995 012Package Change  
8/12/1993 011Control Supplement  
1/12/1993 010Control Supplement  
4/29/1985 009Labeling Revision  
5/13/1983 008Control Supplement  
4/18/1983 007Control Supplement  
11/21/1978 005Labeling Revision  
6/7/1978 002Control Supplement  
10/11/1978 001Manufacturing Change or Addition  
11/16/1976 000Approval  
 
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