ERYTHROCIN(ERYTHROMYCIN LACTOBIONATE) - 美国FDA药品数据库

药品名称	ERYTHROCIN
申请号	050182	产品号	002
活性成分	ERYTHROMYCIN LACTOBIONATE	市场状态	停止上市
剂型或给药途径	INJECTABLE;INJECTION	规格	EQ 500MG BASE/VIAL
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		审评分类

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
050182	125	AP	Letter	2004/09/17	下载
050182	122	AP	Letter	2002/05/23	下载

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
050182	125	AP	2004/09/16	Labeling Revision
050182	124	AP	2002/12/13	Expiration Date Change
050182	123	AP	2002/08/29	Control Supplement
050182	122	AP	2002/05/23	Labeling Revision
050182	121	AP	1999/04/23	Control Supplement
050182	119	AP	1997/10/27	Package Change
050182	118	AP	1996/03/18	Package Change
050182	117	AP	1983/10/06	Formulation Revision
050182	116	AP	1982/09/23	Control Supplement
050182	115	AP	1982/05/21	Control Supplement
050182	114	AP	1982/04/06	Control Supplement
050182	113	AP	1981/11/10	Package Change
050182	112	AP	1981/10/07	Labeling Revision
050182	111	AP	1981/09/16	Control Supplement
050182	110	AP	1981/06/05	Control Supplement
050182	109	AP	1981/05/20	Package Change
050182	108	AP	1981/05/14	Control Supplement
050182	107	AP	1981/04/28	Control Supplement
050182	106	AP	1981/03/03	Control Supplement
050182	105	AP	1981/01/30	Labeling Revision
050182	104	AP	1980/12/17	Labeling Revision
050182	102	AP	1980/10/21	Labeling Revision
050182	101	AP	1980/10/21	Labeling Revision
050182	100	AP	1980/09/23	Control Supplement
050182	099	AP	1980/09/04	Control Supplement
050182	098	AP	1980/08/19	Labeling Revision
050182	097	AP	1980/07/23	Labeling Revision
050182	096	AP	1980/07/17	Labeling Revision
050182	095	AP	1980/07/15	Labeling Revision
050182	094	AP	1980/06/26	Labeling Revision
050182	093	AP	1980/05/23	Labeling Revision
050182	092	AP	1980/05/21	Control Supplement
050182	091	AP	1980/05/22	Control Supplement
050182	090	AP	1980/05/07	Control Supplement
050182	089	AP	1980/05/06	Labeling Revision
050182	088	AP	1980/05/06	Labeling Revision
050182	087	AP	1980/05/07	Formulation Revision
050182	086	AP	1980/04/25	Control Supplement
050182	085	AP	1980/03/26	Control Supplement
050182	084	AP	1980/03/25	Labeling Revision
050182	083	AP	1980/03/25	Control Supplement
050182	082	AP	1980/03/17	Labeling Revision
050182	081	AP	1980/03/12	Control Supplement
050182	080	AP	1980/02/15	Formulation Revision
050182	079	AP	1980/01/14	Labeling Revision
050182	078	AP	1980/01/04	Formulation Revision
050182	077	AP	1980/01/16	Expiration Date Change
050182	076	AP	1979/12/17	Control Supplement
050182	075	AP	1979/11/23	Formulation Revision
050182	074	AP	1979/11/06	Labeling Revision
050182	073	AP	1979/11/06	Labeling Revision
050182	072	AP	1979/09/18	Control Supplement
050182	071	AP	1979/08/27	Formulation Revision
050182	070	AP	1979/08/22	Control Supplement
050182	069	AP	1979/10/10	Control Supplement
050182	068	AP	1979/06/20	Control Supplement
050182	067	AP	1979/06/19	Control Supplement
050182	066	AP	1979/05/21	Control Supplement
050182	065	AP	1979/05/04	Control Supplement
050182	064	AP	1979/07/19	Package Change
050182	063	AP	1979/04/13	Control Supplement
050182	062	AP	1979/03/29	Control Supplement
050182	061	AP	1979/04/05	Package Change
050182	060	AP	1979/03/20	Labeling Revision
050182	059	AP	1979/03/29	Package Change
050182	058	AP	1979/03/07	Control Supplement
050182	057	AP	1979/03/09	Control Supplement
050182	056	AP	1979/01/19	Labeling Revision
050182	055	AP	1979/01/08	Control Supplement
050182	054	AP	1978/12/13	Control Supplement
050182	053	AP	1978/12/07	Control Supplement
050182	052	AP	1978/12/04	Formulation Revision
050182	050	AP	1978/10/30	Control Supplement
050182	049	AP	1978/09/25	Labeling Revision
050182	048	AP	1978/06/07	Formulation Revision
050182	047	AP	1978/05/25	Control Supplement
050182	046	AP	1977/08/09	Formulation Revision
050182	045	AP	1977/06/10	Control Supplement
050182	043	AP	1975/01/07	Labeling Revision
050182	042	AP	1972/05/17	Labeling Revision
050182	041	AP	1974/05/10	New or Modified Indication
050182	040	AP	1971/11/19	Labeling Revision
050182	039	AP	1971/04/27	Labeling Revision
050182	038	AP	1968/09/19	Labeling Revision
050182	037	AP	1967/06/15	Labeling Revision
050182	036	AP	1967/04/18	Labeling Revision
050182	035	AP	1966/12/30	Formulation Revision
050182	034	AP	1966/12/16	Labeling Revision
050182	033	AP	1966/05/31	Labeling Revision
050182	032	AP	1966/01/14	Labeling Revision
050182	031	AP	1965/10/08	Manufacturing Change or Addition
050182	030	AP	1965/09/15	Labeling Revision
050182	029	AP	1965/10/05	Control Supplement
050182	028	AP	1993/03/12	Labeling Revision
050182	027	AP	1996/10/11	Labeling Revision
050182	026	AP	1991/12/05	Chemistry Generic
050182	023	AP	1991/05/03	Labeling Revision
050182	022	AP	1988/11/30	Control Supplement
050182	021	AP	1987/12/30	Labeling Revision
050182	020	AP	1965/05/11	Labeling Revision
050182	019	AP	1965/05/04	Labeling Revision
050182	018	AP	1965/02/10	Labeling Revision
050182	016	AP	1964/10/27	Labeling Revision
050182	015	AP	1964/10/26	Labeling Revision
050182	014	AP	1984/05/16	Control Supplement
050182	013	AP	1984/09/25	Control Supplement
050182	012	AP	1983/12/20	Formulation Revision
050182	011	AP	1983/11/09	Labeling Revision
050182	010	AP	1983/11/01	Labeling Revision
050182	009	AP	1983/07/22	Manufacturing Change or Addition
050182	008	AP	1983/06/02	Control Supplement
050182	007	AP	1983/05/27	Control Supplement
050182	006	AP	1964/09/22	Labeling Revision
050182	005	AP	1964/08/20	Labeling Revision
050182	004	AP	1964/08/05	Labeling Revision
050182	003	AP	1964/07/17	Labeling Revision
050182	002	AP	1982/10/08	Control Supplement
050182	001	AP	1964/07/13	Labeling Revision
050182	000	AP	1964/06/25	Approval

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