美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=PERMITIL"
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
PERMITIL 012034 001 NDA FLUPHENAZINE HYDROCHLORIDE TABLET;ORAL 0.25MG No No 1959/09/09 Approved Prior to Jan 1, 1982 SCHERING Discontinued
PERMITIL 012034 004 NDA FLUPHENAZINE HYDROCHLORIDE TABLET;ORAL 2.5MG No No 1959/09/09 Approved Prior to Jan 1, 1982 SCHERING Discontinued
PERMITIL 012034 005 NDA FLUPHENAZINE HYDROCHLORIDE TABLET;ORAL 5MG No No 1959/09/09 Approved Prior to Jan 1, 1982 SCHERING Discontinued
PERMITIL 012034 006 NDA FLUPHENAZINE HYDROCHLORIDE TABLET;ORAL 10MG No No 1959/09/09 Approved Prior to Jan 1, 1982 SCHERING Discontinued
PERMITIL 012419 004 NDA FLUPHENAZINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1MG No No 1960/06/24 Approved Prior to Jan 1, 1982 SCHERING Discontinued
PERMITIL 016008 001 NDA FLUPHENAZINE HYDROCHLORIDE CONCENTRATE;ORAL 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** No No 1965/04/07 Approved Prior to Jan 1, 1982 SCHERING Discontinued
药品名称,活性成分,申请号搜索 高级检索
©2006-2019 DrugFuture->U.S. FDA Drugs Database