Visitor Monitoring Drug History: KADIAN
 
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: KADIAN
FDA Application No: (NDA) 020616
Active Ingredient(s): MORPHINE SULFATE
Company: ALPHARMA PHARMS
 
Label History
 
View the label approved on April 25, 2007 for KADIAN, (NDA) 020616


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
4/20/2007 025Formulation Revision Letter
Label 
10/27/2006 022Formulation Revision Letter
Label 
2/27/2007 021Labeling Revision Letter
Label 
2/27/2007 017Formulation Revision Letter
Label 
9/28/2005 010Package Change Letter
Label 
3/28/2002 009Control Supplement  
12/18/2001 008Control Supplement  
12/21/2001 007Control Supplement  
2/8/2001 006Manufacturing Change or Addition  
2/28/2000 005Formulation Revision  
3/9/2001 004Control Supplement  
7/16/1999 003Labeling Revision  
4/8/1998 002Package Change  
7/29/1997 001Labeling Revision  
7/3/1996 000Approval  
 
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