Visitor Monitoring Drug History: LAMISIL
 
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: LAMISIL
FDA Application No: (NDA) 020749
Active Ingredient(s): TERBINAFINE HYDROCHLORIDE
Company: NOVARTIS
 
Label History
 
View the label approved on March 28, 2003 for LAMISIL, (NDA) 020749


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
8/2/2002 008Package Change  
1/22/2002 007Manufacturing Change or Addition  
12/27/2001 006Manufacturing Change or Addition  
4/30/2001 005Control Supplement  
3/27/2003 004Labeling Revision Letter
Label 
5/13/1999 002Manufacturing Change or Addition  
10/17/1997 000Approval Review 
 
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