Visitor Monitoring Drug History: ZONEGRAN
 
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: ZONEGRAN
FDA Application No: (NDA) 020789
Active Ingredient(s): ZONISAMIDE
Company: DAINIPPON
 
Label History
 
View the label approved on November 22, 2006 for ZONEGRAN, (NDA) 020789


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
11/20/2006 019Labeling Revision Letter
Label 
6/13/2002 008Control Supplement  
5/15/2002 007Manufacturing Change or Addition  
4/1/2002 006Manufacturing Change or Addition  
10/7/2002 005Labeling Revision Letter
Label 
2/6/2002 004Manufacturing Change or Addition  
11/28/2001 003Control Supplement  
12/4/2000 002Manufacturing Change or Addition  
8/22/2003 001Manufacturing Change or Addition Letter
Label 
3/27/2000 000Approval Letter
Label
Review
Consumer Information Sheet 
 
Therapeutic Equivalents
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