美国FDA药品数据库-药物在线

商品名	申请号	产品号	申请类型	活性成分	剂型/给药途径	规格/剂量	RLD	RS	申请号原始批准/暂定批准日期	产品号批准日期	申请人	市场状态
HYDERGINE	009087	001	NDA	ERGOLOID MESYLATES	TABLET;SUBLINGUAL	1MG	No	No	1953/11/05	Approved Prior to Jan 1, 1982	NOVARTIS	Discontinued
HYDERGINE	009087	002	NDA	ERGOLOID MESYLATES	TABLET;SUBLINGUAL	0.5MG	No	No	1953/11/05	Approved Prior to Jan 1, 1982	NOVARTIS	Discontinued
HYDERGINE	017993	001	NDA	ERGOLOID MESYLATES	TABLET;ORAL	1MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1977/12/30	Approved Prior to Jan 1, 1982	NOVARTIS	Discontinued
HYDERGINE	017993	003	NDA	ERGOLOID MESYLATES	TABLET;ORAL	0.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1977/12/30	Approved Prior to Jan 1, 1982	NOVARTIS	Discontinued
HYDERGINE	018418	001	NDA	ERGOLOID MESYLATES	SOLUTION;ORAL	1MG/ML	No	No	1981/01/30	Approved Prior to Jan 1, 1982	NOVARTIS	Discontinued
HYDERGINE LC	018706	001	NDA	ERGOLOID MESYLATES	CAPSULE;ORAL	1MG	No	No	1983/01/18	1983/01/18	NOVARTIS	Discontinued