Visitor Monitoring Drug History: ZOFRAN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: ZOFRAN
FDA Application No: (NDA) 020605
Active Ingredient(s): ONDANSETRON HYDROCHLORIDE
Company: GLAXOSMITHKLINE
 
Label History
 
View the label approved on August 23, 2006 for ZOFRAN, (NDA) 020605


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
8/22/2006 010Labeling Revision Letter
Label 
12/27/2005 008Labeling Revision Letter
Label 
11/24/2004 007Labeling Revision Letter
Label 
12/13/2000 005Labeling Revision Letter
Label 
4/11/2000 004Labeling Revision Review 
1/26/1999 003Manufacturing Change or Addition  
4/15/1997 001Labeling Revision  
1/24/1997 000Approval Review 
 
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