Visitor Monitoring Drug History: MIACALCIN
 
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: MIACALCIN
FDA Application No: (NDA) 017808
Active Ingredient(s): CALCITONIN, SALMON
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for MIACALCIN, (NDA) 017808
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/3/2003 024Labeling Revision Letter 
2/12/2002 022Manufacturing Change or Addition  
11/2/2001 020Manufacturing Change or Addition  
7/23/1999 018Control Supplement  
5/26/1999 017Manufacturing Change or Addition  
1/13/1999 016Manufacturing Change or Addition  
12/24/1998 015Manufacturing Change or Addition  
7/14/1997 014Labeling Revision Review 
8/1/1997 013Control Supplement  
1/2/1997 012Manufacturing Change or Addition  
8/14/1996 011Manufacturing Change or Addition  
6/9/1995 010Control Supplement  
8/5/1992 009Package Change  
2/22/1993 008Control Supplement  
6/1/1992 007Labeling Revision  
6/10/1992 006Labeling Revision  
7/22/1994 005Control Supplement  
6/26/1992 004Manufacturing Change or Addition  
3/26/1993 003Labeling Revision  
10/3/1991 002Labeling Revision  
3/29/1991 001Formulation Revision  
7/3/1986 000Approval  
 
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