Visitor Monitoring Drug History: PHOSPHOTEC
 
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: PHOSPHOTEC
FDA Application No: (NDA) 017680
Active Ingredient(s): TECHNETIUM TC-99M PYROPHOSPHATE KIT
Company: BRACCO
 
Label History
 
Labels are not available on this site for PHOSPHOTEC, (NDA) 017680
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/14/1999 012Manufacturing Change or Addition  
3/21/1994 011Control Supplement  
5/9/1988 010Labeling Revision  
9/30/1985 009Manufacturing Change or Addition  
8/30/1982 008Labeling Revision  
5/6/1983 006Practioner Draft Labeling  
2/4/1982 005Labeling Revision  
2/4/1982 004Labeling Revision  
7/14/1977 003Labeling Revision  
4/17/1978 002Labeling Revision  
12/20/1976 001Manufacturing Change or Addition  
10/20/1976 000Approval  
 
Therapeutic Equivalents
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