美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=EVEKEO ODT"
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
EVEKEO ODT 209905 001 NDA AMPHETAMINE SULFATE TABLET, ORALLY DISINTEGRATING;ORAL 5MG Yes No 2019/01/30 2019/01/30 AZURITY Discontinued
EVEKEO ODT 209905 002 NDA AMPHETAMINE SULFATE TABLET, ORALLY DISINTEGRATING;ORAL 10MG Yes No 2019/01/30 2019/01/30 AZURITY Discontinued
EVEKEO ODT 209905 003 NDA AMPHETAMINE SULFATE TABLET, ORALLY DISINTEGRATING;ORAL 15MG Yes No 2019/01/30 2019/01/30 AZURITY Discontinued
EVEKEO ODT 209905 004 NDA AMPHETAMINE SULFATE TABLET, ORALLY DISINTEGRATING;ORAL 20MG Yes No 2019/01/30 2019/01/30 AZURITY Discontinued
EVEKEO ODT 209905 005 NDA AMPHETAMINE SULFATE TABLET, ORALLY DISINTEGRATING;ORAL 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 2019/01/30 2021/04/16 AZURITY Discontinued
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