Visitor Monitoring Drug History: ULTRA-TECHNEKOW FM
 
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: ULTRA-TECHNEKOW FM
FDA Application No: (NDA) 017243
Active Ingredient(s): TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR
Company: MALLINCKRODT
 
Label History
 
View the label approved on October 22, 2004 for ULTRATECHNEKOW FM, (NDA) 017243


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/27/2006 028Labeling Revision Letter 
10/15/2004 025Control Supplement Letter
Label 
1/16/2003 022Control Supplement Letter 
4/19/2002 021Manufacturing Change or Addition  
3/4/2002 020Control Supplement  
12/29/1999 019Formulation Revision  
4/14/1999 018Control Supplement  
11/20/1998 017Manufacturing Change or Addition  
2/18/1998 016Labeling Revision  
6/18/1997 015Manufacturing Change or Addition  
8/20/1996 014Control Supplement  
3/21/1997 013Control Supplement  
7/16/1996 012Control Supplement  
3/26/1984 010Practioner Draft Labeling  
6/30/1982 009Package Change  
5/7/1982 008Control Supplement  
7/24/1979 006Package Change  
8/23/1977 005Manufacturing Change or Addition  
7/27/1977 004Manufacturing Change or Addition  
10/8/1976 003Package Change  
11/23/1973 000Approval  
 
There are no Therapeutic Equivalents
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