Visitor Monitoring Drug History: SANDIMMUNE
 
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: SANDIMMUNE
FDA Application No: (NDA) 050573
Active Ingredient(s): CYCLOSPORINE
Company: NOVARTIS
 
Label History
 
View the label approved on March 10, 2006 for SANDIMMUNE, (NDA) 050573


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
3/6/2006 031Labeling Revision Letter
Label 
7/19/2005 030Labeling Revision Letter
Label 
2/6/2004 028Labeling Revision Letter
Label 
2/6/2004 027Labeling Revision Letter
Label 
4/12/2002 025Manufacturing Change or Addition  
1/16/2002 024Manufacturing Change or Addition  
2/14/2003 023Labeling Revision Letter
Label 
3/5/2003 021Labeling Revision Letter
Label 
3/9/2001 020Control Supplement  
4/4/2001 019Manufacturing Change or Addition  
10/4/2000 018Labeling Revision  
12/21/1999 017Labeling Revision  
5/13/1999 016Manufacturing Change or Addition  
10/20/1998 015Manufacturing Change or Addition  
3/30/1998 014Manufacturing Change or Addition  
8/2/1996 013Control Supplement  
8/9/1996 012Labeling Revision  
11/10/1994 011Labeling Revision  
3/7/1995 010Manufacturing Change or Addition  
5/9/1994 009Control Supplement  
5/9/1994 008Control Supplement  
3/19/1993 007Control Supplement  
2/21/1992 006Control Supplement  
6/10/1991 005Labeling Revision  
3/19/1993 004Expiration Date Change  
3/19/1993 003Control Supplement  
11/14/1983 000Approval  
 
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