Visitor Monitoring Drug History: CALCIMAR
 
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: CALCIMAR
FDA Application No: (NDA) 017769
Active Ingredient(s): CALCITONIN, SALMON
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for CALCIMAR, (NDA) 017769
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/16/1996 027Control Supplement  
7/6/1993 025Labeling Revision  
9/24/1993 024Labeling Revision  
7/12/1993 023Control Supplement  
5/6/1992 022Labeling Revision  
6/1/1992 021Labeling Revision  
4/8/1991 020Labeling Revision  
4/4/1991 019Manufacturing Change or Addition  
3/21/1990 018Control Supplement  
7/6/1989 017Labeling Revision  
3/22/1988 016Labeling Revision  
8/8/1986 014Expiration Date Change  
5/10/1984 013Control Supplement  
12/21/1984 012Labeling Revision  
12/21/1984 008Labeling Revision  
5/4/1979 005Control Supplement  
4/6/1979 004Control Supplement  
1/10/1979 003Control Supplement  
11/26/1979 002Labeling Revision  
8/14/1978 001Control Supplement  
4/17/1978 000Approval  
 
Therapeutic Equivalents
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