TUBOCURARINE CHLORIDE(TUBOCURARINE CHLORIDE)

药品名称	TUBOCURARINE CHLORIDE
申请号	006095	产品号	001
活性成分	TUBOCURARINE CHLORIDE	市场状态	停止上市
剂型或给药途径	INJECTABLE;INJECTION	规格	3MG/ML
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	HOSPIRA INC
化学类型	New formulation or new manufacturer	审评分类	Standard 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
006095	038	AP	1999/02/26	Labeling Revision
006095	037	AP	1998/07/02	Manufacturing Change or Addition
006095	036	AP	1997/10/27	Package Change
006095	035	AP	1994/05/27	Manufacturing Change or Addition
006095	034	AP	1999/02/26	Labeling Revision
006095	033	AP	1990/02/26	Control Supplement
006095	032	AP	1990/03/13	Control Supplement
006095	031	AP	1993/11/09	Control Supplement
006095	030	AP	1988/02/04	Labeling Revision
006095	029	AP	1988/05/31	Manufacturing Change or Addition
006095	028	AP	1984/07/03	Control Supplement
006095	027	AP	1982/05/05	Labeling Revision
006095	026	AP	1986/06/18	Practioner Draft Labeling
006095	025	AP	1982/01/06	Labeling Revision
006095	024	AP	1981/04/14	Control Supplement
006095	023	AP	1981/05/16	Package Change
006095	022	AP	1981/03/06	Control Supplement
006095	020	AP	1980/07/25	Control Supplement
006095	019	AP	1980/07/25	Control Supplement
006095	018	AP	1980/10/01	Control Supplement
006095	017	AP	1980/10/01	Labeling Revision
006095	016	AP	1980/04/30	Labeling Revision
006095	015	AP	1980/05/01	Labeling Revision
006095	014	AP	1980/05/01	Control Supplement
006095	013	AP	1978/06/19	Labeling Revision
006095	012	AP	1977/10/14	Control Supplement
006095	011	AP	1977/06/09	Manufacturing Change or Addition
006095	009	AP	1977/09/06	Formulation Revision
006095	008	AP	1977/09/06	Labeling Revision
006095	007	AP	1977/09/06	Control Supplement
006095	006	AP	1976/07/16	Package Change
006095	005	AP	1975/04/28	Labeling Revision
006095	001	AP	1973/10/29	Labeling Revision
006095	000	AP	1947/01/30	Approval