Visitor Monitoring Drug History: KINEVAC
 
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: KINEVAC
FDA Application No: (NDA) 017697
Active Ingredient(s): SINCALIDE
Company: BRACCO
 
Label History
 
Labels are not available on this site for KINEVAC, (NDA) 017697
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/26/2005 017Labeling Revision Letter 
11/27/2002 015Control Supplement Letter 
11/27/2002 014Package Change Letter 
11/27/2002 013Formulation Revision Letter 
11/27/2002 012Manufacturing Change or Addition Letter 
10/29/2002 011Manufacturing Change or Addition  
12/22/1992 010Labeling Revision  
5/25/1988 009Labeling Revision  
7/15/1985 006Manufacturing Change or Addition  
8/25/1986 005New or Modified Indication  
10/18/1979 004Control Supplement  
9/14/1977 001Control Supplement  
7/21/1976 000Approval  
 
There are no Therapeutic Equivalents
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