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

药品名称	HYDERGINE
申请号	017993	产品号	003
活性成分	ERGOLOID MESYLATES	市场状态	停止上市
剂型或给药途径	TABLET;ORAL	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 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

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
017993	035	AP	2001/04/02	Manufacturing Change or Addition
017993	034	AP	2000/08/01	Manufacturing Change or Addition
017993	033	AP	2000/05/10	Manufacturing Change or Addition
017993	032	AP	2000/03/13	Manufacturing Change or Addition
017993	031	AP	1996/06/18	Control Supplement
017993	029	AP	1995/12/07	Manufacturing Change or Addition
017993	028	AP	1995/10/12	Control Supplement
017993	027	AP	1998/11/12	Labeling Revision
017993	026	AP	1993/09/14	Package Change
017993	023	AP	1994/02/28	Control Supplement
017993	021	AP	1994/02/28	Control Supplement
017993	020	AP	1989/11/07	Package Change
017993	019	AP	1987/05/26	Control Supplement
017993	017	AP	1985/02/07	Expiration Date Change
017993	016	AP	1983/10/26	Labeling Revision
017993	014	AP	1983/02/03	Labeling Revision
017993	012	AP	1982/09/15	Control Supplement
017993	011	AP	1983/01/19	Manufacturing Change or Addition
017993	010	AP	1982/03/25	Package Change
017993	009	AP	1981/08/10	Manufacturing Change or Addition
017993	008	AP	1981/09/02	Control Supplement
017993	007	AP	1981/02/03	Package Change
017993	005	AP	1979/12/11	Manufacturing Change or Addition
017993	004	AP	1981/02/04	Labeling Revision
017993	003	AP	1979/04/05	Manufacturing Change or Addition
017993	002	AP	1979/08/01	Manufacturing Change or Addition
017993	001	AP	1978/06/30	Package Change
017993	000	AP	1977/12/30	Approval