Visitor Monitoring Drug History: CASODEX
 
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: CASODEX
FDA Application No: (NDA) 020498
Active Ingredient(s): BICALUTAMIDE
Company: ASTRAZENECA
 
Label History
 
View the label approved on March 14, 2006 for CASODEX, (NDA) 020498


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
3/10/2006 018Labeling Revision Letter
Label 
5/11/2005 016Labeling Revision Letter
Label 
9/23/2002 013Manufacturing Change or Addition  
1/25/2002 011Control Supplement  
10/25/2001 010Manufacturing Change or Addition  
2/28/2001 008Labeling Revision  
12/11/2000 007Manufacturing Change or Addition  
11/4/1999 005Manufacturing Change or Addition  
12/12/1997 004New or Modified Indication  
11/12/1997 003Control Supplement  
10/4/1995 000Approval  
 
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