美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=TEVETEN"
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
TEVETEN 020738 004 NDA EPROSARTAN MESYLATE TABLET;ORAL EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1997/12/22 1997/12/22 ABBVIE Discontinued
TEVETEN 020738 005 NDA EPROSARTAN MESYLATE TABLET;ORAL EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1997/12/22 1997/12/22 ABBVIE Discontinued
TEVETEN 020738 006 NDA EPROSARTAN MESYLATE TABLET;ORAL EQ 600MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1997/12/22 1999/05/27 ABBVIE Discontinued
TEVETEN HCT 021268 001 NDA EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE TABLET;ORAL 600MG;12.5MG No No 2001/11/01 2001/11/01 ABBVIE Discontinued
TEVETEN HCT 021268 002 NDA EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE TABLET;ORAL 600MG;25MG No No 2001/11/01 2001/11/01 ABBVIE Discontinued
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