QUESTRAN(CHOLESTYRAMINE) - 美国FDA药品数据库

药品名称	QUESTRAN
申请号	016640	产品号	003
活性成分	CHOLESTYRAMINE	市场状态	停止上市
剂型或给药途径	POWDER;ORAL	规格	EQ 4GM RESIN/SCOOPFUL Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons
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	BRISTOL MYERS CO
化学类型	New dosage form	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

与本品相关的市场独占权保护信息
独占权代码	失效日期
无
历史市场独占权保护信息
无

与药品注册相关的信息
申请号	修订号	审批结论	公开文档类型	文档创建时间	获取文档
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
016640	074	AP	1997/08/22	Labeling Revision
016640	071	AP	1994/12/12	Labeling Revision
016640	070	AP	1994/12/12	Labeling Revision
016640	069	AP	1995/09/22	Labeling Revision
016640	068	AP	1995/09/22	Labeling Revision
016640	067	AP	1993/01/07	Control Supplement
016640	066	AP	1992/08/11	Labeling Revision
016640	065	AP	1992/09/22	Control Supplement
016640	063	AP	1991/09/10	Labeling Revision
016640	060	AP	1991/10/24	Labeling Revision
016640	059	AP	1990/05/25	Control Supplement
016640	058	AP	1990/03/05	Control Supplement
016640	057	AP	1991/03/06	Control Supplement
016640	056	AP	1990/02/02	Manufacturing Change or Addition
016640	055	AP	1989/11/28	Labeling Revision
016640	054	AP	1990/01/22	Formulation Revision
016640	050	AP	1989/02/23	Control Supplement
016640	049	AP	1988/12/01	Control Supplement
016640	048	AP	1988/10/11	Package Change
016640	047	AP	1988/08/26	Manufacturing Change or Addition
016640	046	AP	1988/08/26	Package Change
016640	045	AP	1988/07/14	Manufacturing Change or Addition
016640	044	AP	1988/07/14	Manufacturing Change or Addition
016640	043	AP	1988/07/14	Control Supplement
016640	042	AP	1989/03/02	Manufacturing Change or Addition
016640	040	AP	1988/06/29	Manufacturing Change or Addition
016640	039	AP	1988/03/25	Formulation Revision
016640	038	AP	1988/03/18	Control Supplement
016640	037	AP	1988/01/05	Formulation Revision
016640	036	AP	1988/02/16	Manufacturing Change or Addition
016640	035	AP	1987/11/19	Manufacturing Change or Addition
016640	034	AP	1987/11/19	Control Supplement
016640	033	AP	1994/12/07	Labeling Revision
016640	030	AP	1987/09/18	Manufacturing Change or Addition
016640	028	AP	1986/01/24	Control Supplement
016640	027	AP	1986/02/25	Labeling Revision
016640	026	AP	1986/09/19	Control Supplement
016640	025	AP	1986/03/12	Control Supplement
016640	024	AP	1985/09/12	Control Supplement
016640	023	AP	1985/11/26	Formulation Revision
016640	022	AP	1985/11/01	Control Supplement
016640	021	AP	1984/12/21	Labeling Revision
016640	017	AP	1984/05/11	Labeling Revision
016640	016	AP	1984/06/14	Control Supplement
016640	014	AP	1983/11/30	Labeling Revision
016640	013	AP	1983/06/24	Labeling Revision
016640	012	AP	1982/08/16	Control Supplement
016640	011	AP	1982/07/26	Control Supplement
016640	010	AP	1982/06/16	Package Change
016640	009	AP	1981/07/08	Labeling Revision
016640	005	AP	1977/02/17	Labeling Revision
016640	000	AP	1973/08/03	Approval

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