美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SERENTIL"
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
SERENTIL 016774 001 NDA MESORIDAZINE BESYLATE TABLET;ORAL EQ 10MG BASE No No 1970/02/27 Approved Prior to Jan 1, 1982 NOVARTIS Discontinued
SERENTIL 016774 002 NDA MESORIDAZINE BESYLATE TABLET;ORAL EQ 25MG BASE No No 1970/02/27 Approved Prior to Jan 1, 1982 NOVARTIS Discontinued
SERENTIL 016774 003 NDA MESORIDAZINE BESYLATE TABLET;ORAL EQ 50MG BASE No No 1970/02/27 Approved Prior to Jan 1, 1982 NOVARTIS Discontinued
SERENTIL 016774 004 NDA MESORIDAZINE BESYLATE TABLET;ORAL EQ 100MG BASE No No 1970/02/27 Approved Prior to Jan 1, 1982 NOVARTIS Discontinued
SERENTIL 016775 001 NDA MESORIDAZINE BESYLATE INJECTABLE;INJECTION EQ 25MG BASE/ML No No 1970/02/27 Approved Prior to Jan 1, 1982 NOVARTIS Discontinued
SERENTIL 016997 001 NDA MESORIDAZINE BESYLATE CONCENTRATE;ORAL EQ 25MG BASE/ML No No 1972/01/31 Approved Prior to Jan 1, 1982 NOVARTIS Discontinued
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