美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SUBUTEX"
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
SUBUTEX 020732 002 NDA BUPRENORPHINE HYDROCHLORIDE TABLET;SUBLINGUAL EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 2002/10/08 2002/10/08 INDIVIOR INC Discontinued
SUBUTEX 020732 003 NDA BUPRENORPHINE HYDROCHLORIDE TABLET;SUBLINGUAL EQ 8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 2002/10/08 2002/10/08 INDIVIOR INC Discontinued
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