Visitor Monitoring Drug History: ZANAFLEX
 
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: ZANAFLEX
FDA Application No: (NDA) 020397
Active Ingredient(s): TIZANIDINE HYDROCHLORIDE
Company: ACORDA
 
Label History
 
View the label approved on August 4, 2006 for ZANAFLEX, (NDA) 020397


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
7/28/2006 021Labeling Revision Letter
Label 
5/17/2002 016Manufacturing Change or Addition  
4/10/2002 015Expiration Date Change  
11/27/2002 014Labeling Revision Letter 
8/22/2001 013Manufacturing Change or Addition  
8/21/2001 012Manufacturing Change or Addition  
3/20/2001 011Manufacturing Change or Addition  
12/7/2000 010Manufacturing Change or Addition  
8/21/2000 008Manufacturing Change or Addition  
6/26/2000 007Manufacturing Change or Addition  
6/15/1999 005Manufacturing Change or Addition  
2/4/2000 004Manufacturing Change or Addition Review 
10/23/1997 003Manufacturing Change or Addition  
9/2/1997 002Package Change  
9/2/1997 001Control Supplement  
11/27/1996 000Approval  
 
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