LIORESAL(BACLOFEN) - 美国FDA药品数据库

药品名称	LIORESAL
申请号	017851	产品号	001
活性成分	BACLOFEN	市场状态	停止上市
剂型或给药途径	TABLET;ORAL	规格	10MG
治疗等效代码		参比药物	否
批准日期	Approved Prior to Jan 1, 1982	申请机构	NOVARTIS PHARMACEUTICALS CORP
化学类型	New molecular entity (NME)	审评分类	Priority review drug

与本品相关的专利信息（来自橙皮书Orange Book）
专利号	专利过期日	是否化合物专利	是否产品专利	专利用途代码	专利下载
无
历史专利信息
无

药品注册审批历史信息
申请号	修订号	审批结论	审批日期	审批内容
017851	041	AP	2000/04/11	Manufacturing Change or Addition
017851	040	AP	1999/04/21	Package Change
017851	039	AP	1995/08/18	Package Change
017851	038	AP	1995/08/18	Control Supplement
017851	036	AP	1990/04/05	Package Change
017851	034	AP	1989/11/17	Labeling Revision
017851	031	AP	1989/04/07	Package Change
017851	029	AP	1985/05/14	Manufacturing Change or Addition
017851	028	AP	1984/11/16	Control Supplement
017851	027	AP	1984/02/28	Manufacturing Change or Addition
017851	026	AP	1984/02/15	Control Supplement
017851	025	AP	1986/02/28	Labeling Revision
017851	024	AP	1984/03/21	Labeling Revision
017851	023	AP	1983/03/07	Control Supplement
017851	022	AP	1982/10/18	Package Change
017851	021	AP	1982/03/18	Package Change
017851	019	AP	1983/03/02	Labeling Revision
017851	017	AP	1985/01/24	Control Supplement
017851	016	AP	1981/09/24	Formulation Revision
017851	015	AP	1982/01/20	Labeling Revision
017851	014	AP	1981/05/14	Formulation Revision
017851	013	AP	1981/05/14	Expiration Date Change
017851	012	AP	1981/04/21	Package Change
017851	011	AP	1980/10/06	Package Change
017851	009	AP	1980/05/23	Manufacturing Change or Addition
017851	008	AP	1980/03/19	Labeling Revision
017851	007	AP	1981/02/03	Package Change
017851	006	AP	1979/04/13	Package Change
017851	005	AP	1979/12/31	Control Supplement
017851	004	AP	1979/12/31	Control Supplement
017851	003	AP	1979/03/21	Package Change
017851	002	AP	1978/05/16	Expiration Date Change
017851	001	AP	1978/04/04	Labeling Revision
017851	000	AP	1977/11/22	Approval