Drug History: LAMISIL

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9

Label and Approval History

Drug Name:	LAMISIL
FDA Application No:	(NDA) 020980
Active Ingredient(s):	TERBINAFINE HYDROCHLORIDE
Company:	NOVARTIS

Label History

View the label approved on July 27, 2007 for LAMISIL, (NDA) 020980

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 Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
7/25/2007	005	Labeling Revision	Letter Label
5/9/2001	003	Control Supplement
9/3/1999	002	Manufacturing Change or Addition
7/22/1999	001	Package Change
3/9/1999	000	Approval	Letter Review Dear Health Professional Letter

Therapeutic Equivalents