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) 020192
Active Ingredient(s): TERBINAFINE HYDROCHLORIDE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for LAMISIL, (NDA) 020192
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/3/1998 014Control Supplement  
6/30/1997 013Control Supplement  
4/3/1997 012Control Supplement  
1/21/1997 011Control Supplement  
10/4/1996 010Manufacturing Change or Addition  
12/6/1996 009Control Supplement  
8/8/1996 007Control Supplement  
11/2/1995 006Manufacturing Change or Addition  
10/17/1995 005Control Supplement  
4/25/1995 004Control Supplement  
1/21/1997 003New or Modified Indication  
8/4/1993 002Manufacturing Change or Addition  
12/30/1992 000Approval  
 
Therapeutic Equivalents
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