美国FDA药品数据库-药物在线

商品名	申请号	产品号	申请类型	活性成分	剂型/给药途径	规格/剂量	RLD	RS	申请号原始批准/暂定批准日期	产品号批准日期	申请人	市场状态
LAMISIL	020192	001	NDA	TERBINAFINE HYDROCHLORIDE	CREAM;TOPICAL	1% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1992/12/30	1992/12/30	NOVARTIS	Discontinued
LAMISIL	020539	001	NDA	TERBINAFINE HYDROCHLORIDE	TABLET;ORAL	EQ 250MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1996/05/10	1996/05/10	NOVARTIS	Discontinued
LAMISIL	020749	001	NDA	TERBINAFINE HYDROCHLORIDE	SOLUTION;TOPICAL	1%	No	No	1997/10/17	1997/10/17	KARO HLTHCARE	Discontinued
LAMISIL	020846	001	NDA	TERBINAFINE	GEL;TOPICAL	1%	No	No	1998/04/29	1998/04/29	KARO HLTHCARE	Discontinued
LAMISIL	020980	001	NDA	TERBINAFINE HYDROCHLORIDE	CREAM;TOPICAL	1%	Yes	Yes	1999/03/09	1999/03/09	KARO HLTHCARE	Over-the-counter
LAMISIL AT	021124	001	NDA	TERBINAFINE HYDROCHLORIDE	SOLUTION;TOPICAL	1%	Yes	Yes	2000/03/17	2000/03/17	KARO HLTHCARE	Over-the-counter
LAMISIL AT	021124	002	NDA	TERBINAFINE HYDROCHLORIDE	SPRAY;TOPICAL	1%	Yes	Yes	2000/03/17	2000/03/17	KARO HLTHCARE	Over-the-counter
LAMISIL AT	021958	001	NDA	TERBINAFINE	GEL;TOPICAL	1%	Yes	Yes	2006/07/24	2006/07/24	KARO HLTHCARE	Over-the-counter
LAMISIL	022071	001	NDA	TERBINAFINE HYDROCHLORIDE	GRANULE;ORAL	EQ 125MG BASE/PACKET	Yes	No	2007/09/28	2007/09/28	NOVARTIS	Discontinued
LAMISIL	022071	002	NDA	TERBINAFINE HYDROCHLORIDE	GRANULE;ORAL	EQ 187.5MG BASE/PACKET	Yes	No	2007/09/28	2007/09/28	NOVARTIS	Discontinued