美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=HEXADROL"
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
HEXADROL 012674 001 NDA DEXAMETHASONE ELIXIR;ORAL 0.5MG/5ML No No 1960/12/21 Approved Prior to Jan 1, 1982 ASPEN GLOBAL INC Discontinued
HEXADROL 012675 004 NDA DEXAMETHASONE TABLET;ORAL 0.5MG No No 1962/04/20 Approved Prior to Jan 1, 1982 ASPEN GLOBAL INC Discontinued
HEXADROL 012675 007 NDA DEXAMETHASONE TABLET;ORAL 0.75MG No No 1962/04/20 Approved Prior to Jan 1, 1982 ASPEN GLOBAL INC Discontinued
HEXADROL 012675 009 NDA DEXAMETHASONE TABLET;ORAL 1.5MG No No 1962/04/20 Approved Prior to Jan 1, 1982 ASPEN GLOBAL INC Discontinued
HEXADROL 012675 010 NDA DEXAMETHASONE TABLET;ORAL 4MG No No 1962/04/20 Approved Prior to Jan 1, 1982 ASPEN GLOBAL INC Discontinued
HEXADROL 014694 002 NDA DEXAMETHASONE SODIUM PHOSPHATE INJECTABLE;INJECTION EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1964/12/04 Approved Prior to Jan 1, 1982 ASPEN GLOBAL INC Discontinued
HEXADROL 014694 003 NDA DEXAMETHASONE SODIUM PHOSPHATE INJECTABLE;INJECTION EQ 10MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1964/12/04 Approved Prior to Jan 1, 1982 ASPEN GLOBAL INC Discontinued
HEXADROL 014694 004 NDA DEXAMETHASONE SODIUM PHOSPHATE INJECTABLE;INJECTION EQ 20MG PHOSPHATE/ML No No 1964/12/04 Approved Prior to Jan 1, 1982 ASPEN GLOBAL INC Discontinued
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