Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 020192
Company: NOVARTIS

Products on NDA 20192

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
LAMISIL	TERBINAFINE HYDROCHLORIDE	1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	CREAM;TOPICAL	Discontinued	None	No	No