美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=LARODOPA"
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
LARODOPA 016912 001 NDA LEVODOPA CAPSULE;ORAL 250MG No No 1970/06/04 Approved Prior to Jan 1, 1982 ROCHE Discontinued
LARODOPA 016912 002 NDA LEVODOPA CAPSULE;ORAL 100MG No No 1970/06/04 Approved Prior to Jan 1, 1982 ROCHE Discontinued
LARODOPA 016912 003 NDA LEVODOPA TABLET;ORAL 250MG No No 1970/06/04 Approved Prior to Jan 1, 1982 ROCHE Discontinued
LARODOPA 016912 004 NDA LEVODOPA TABLET;ORAL 500MG No No 1970/06/04 Approved Prior to Jan 1, 1982 ROCHE Discontinued
LARODOPA 016912 005 NDA LEVODOPA TABLET;ORAL 100MG No No 1970/06/04 Approved Prior to Jan 1, 1982 ROCHE Discontinued
LARODOPA 016912 006 NDA LEVODOPA CAPSULE;ORAL 500MG No No 1970/06/04 Approved Prior to Jan 1, 1982 ROCHE Discontinued
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