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
TAVIST	017661	001	NDA	CLEMASTINE FUMARATE	TABLET;ORAL	2.68MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1977/02/25	Approved Prior to Jan 1, 1982	NOVARTIS	Discontinued
TAVIST-1	017661	002	NDA	CLEMASTINE FUMARATE	TABLET;ORAL	1.34MG	No	No	1977/02/25	Approved Prior to Jan 1, 1982	NOVARTIS	Discontinued
TAVIST-1	017661	003	NDA	CLEMASTINE FUMARATE	TABLET;ORAL	1.34MG	No	No	1977/02/25	1992/08/21	NOVARTIS	Discontinued
TAVIST	018675	001	NDA	CLEMASTINE FUMARATE	SYRUP;ORAL	EQ 0.5MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1985/06/28	1985/06/28	NOVARTIS	Discontinued
TAVIST-1	020925	001	NDA	CLEMASTINE FUMARATE	TABLET;ORAL	1.34MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1992/08/21	1992/08/21	HALEON US HOLDINGS	Discontinued
TAVIST ALLERGY/SINUS/HEADACHE	021082	001	NDA	ACETAMINOPHEN; CLEMASTINE FUMARATE; PSEUDOEPHEDRINE HYDROCHLORIDE	TABLET;ORAL	500MG;EQ 0.25MG BASE;30MG	No	No	2001/03/01	2001/03/01	NOVARTIS	Discontinued