Visitor Monitoring Drug History: SANDOSTATIN
 
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Label and Approval History

Drug Name: SANDOSTATIN
FDA Application No: (NDA) 019667
Active Ingredient(s): OCTREOTIDE ACETATE
Company: NOVARTIS
 
Label History
 
View the label approved on September 8, 2005 for SANDOSTATIN, (NDA) 019667


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
9/2/2005 050Labeling Revision Letter
Label 
1/17/2003 044Manufacturing Change or Addition Letter
Label 
5/28/2002 043Package Change  
2/10/2003 042Manufacturing Change or Addition Letter 
5/13/2002 041Manufacturing Change or Addition  
1/3/2002 040Manufacturing Change or Addition  
6/21/2001 039Manufacturing Change or Addition  
7/2/2001 038Labeling Revision  
2/17/1999 036Manufacturing Change or Addition  
2/17/1999 035Manufacturing Change or Addition  
7/31/1998 034Manufacturing Change or Addition  
12/17/1998 033Control Supplement  
7/24/2002 032Labeling Revision Letter 
10/24/1997 031Expiration Date Change  
10/24/1997 030Control Supplement  
10/24/1997 029Control Supplement  
7/24/2002 028Labeling Revision Letter 
10/24/1997 027Control Supplement  
10/21/1996 026Control Supplement  
8/14/1996 025Control Supplement  
7/16/1996 024Control Supplement  
6/12/1996 023Manufacturing Change or Addition  
2/16/1996 022Control Supplement  
12/6/1994 021Formulation Revision  
12/18/1995 020Formulation Revision  
2/6/1995 019Control Supplement  
5/3/1994 017New or Modified Indication  
1/12/1993 016Control Supplement  
9/30/1992 015Manufacturing Change or Addition  
7/31/1992 014Labeling Revision  
10/10/1995 012Control Supplement  
11/7/1995 011Control Supplement  
2/28/1992 010Control Supplement  
10/4/1991 008Labeling Revision  
7/3/1991 007Labeling Revision  
4/16/1990 005Labeling Revision  
6/12/1991 004Control Supplement Review 
6/23/1989 003Control Supplement  
10/21/1988 000Approval  
 
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