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) 022071
Active Ingredient(s): TERBINAFINE HYDROCHLORIDE
Company: NOVARTIS
 
Label History
 
View the label approved on October 4, 2007 for LAMISIL, (NDA) 022071


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
9/28/2007 000Approval Letter
Label 
 
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