HYDERGINE(ERGOLOID MESYLATES) - 美国FDA药品数据库

药品名称	HYDERGINE
申请号	009087	产品号	002
活性成分	ERGOLOID MESYLATES	市场状态	停止上市
剂型或给药途径	TABLET;SUBLINGUAL	规格	0.5MG
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	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
009087	047	AP	2000/05/10	Manufacturing Change or Addition
009087	046	AP	1999/04/21	Package Change
009087	045	AP	1998/11/12	Labeling Revision
009087	044	AP	1993/09/14	Package Change
009087	041	AP	1993/04/06	Control Supplement
009087	039	AP	1989/11/07	Package Change
009087	038	AP	1987/05/26	Control Supplement
009087	036	AP	1983/10/26	Labeling Revision
009087	035	AP	1983/08/26	Control Supplement
009087	033	AP	1983/02/03	Labeling Revision
009087	031	AP	1983/01/19	Manufacturing Change or Addition
009087	030	AP	1981/08/10	Manufacturing Change or Addition
009087	029	AP	1981/09/02	Control Supplement
009087	028	AP	1981/01/19	Package Change
009087	027	AP	1981/02/24	Control Supplement
009087	026	AP	1979/12/11	Manufacturing Change or Addition
009087	025	AP	1979/06/14	Package Change
009087	024	AP	1981/02/04	Labeling Revision
009087	022	AP	1978/07/13	Package Change
009087	021	AP	1978/10/16	Manufacturing Change or Addition
009087	020	AP	1978/06/27	Expiration Date Change
009087	019	AP	1978/04/14	Labeling Revision
009087	017	AP	1978/03/20	Package Change
009087	013	AP	1976/07/28	Manufacturing Change or Addition
009087	012	AP	1976/06/30	Package Change
009087	011	AP	1976/02/23	Control Supplement
009087	009	AP	1975/11/13	Control Supplement
009087	008	AP	1975/10/06	Control Supplement
009087	007	AP	1975/06/25	Control Supplement
009087	006	AP	1975/06/02	General Efficacy (MarkIV)
009087	005	AP	1974/12/13	Control Supplement
009087	004	AP	1975/04/16	Other Amendment
009087	002	AP	1974/06/25	Control Supplement
009087	000	AP	1953/11/05	Approval