美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=HYDERGINE"
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017993 001 NDA ERGOLOID MESYLATES TABLET;ORAL 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1977/12/30 Approved Prior to Jan 1, 1982 NOVARTIS Discontinued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NDA ERGOLOID MESYLATES TABLET;ORAL 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1977/12/30 Approved Prior to Jan 1, 1982 NOVARTIS Discontinued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
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