Visitor Monitoring Drug History: KYTRIL
 
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: KYTRIL
FDA Application No: (NDA) 020305
Active Ingredient(s): GRANISETRON HYDROCHLORIDE
Company: ROCHE
 
Label History
 
View the label approved on November 30, 2005 for KYTRIL, (NDA) 020305


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
11/23/2005 010Labeling Revision Letter
Label 
11/25/2002 008Control Supplement  
11/5/2002 006Manufacturing Change or Addition  
11/5/2002 005Manufacturing Change or Addition  
7/27/1999 004New or Modified Indication Letter
Review 
6/15/1998 003Formulation Revision  
10/24/1996 002Manufacturing Change or Addition  
10/6/1997 001New Dosage Regimen Review 
3/16/1995 000Approval  
 
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