美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SOLODYN"
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
SOLODYN 050808 001 NDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 45MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 2006/05/08 2006/05/08 MEDICIS Discontinued
SOLODYN 050808 002 NDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 90MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 2006/05/08 2006/05/08 MEDICIS Discontinued
SOLODYN 050808 003 NDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 135MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 2006/05/08 2006/05/08 MEDICIS Discontinued
SOLODYN 050808 004 NDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 65MG BASE Yes No 2006/05/08 2009/07/23 MEDICIS Prescription
SOLODYN 050808 005 NDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 115MG BASE Yes Yes 2006/05/08 2009/07/23 MEDICIS Prescription
SOLODYN 050808 006 NDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 105MG BASE Yes No 2006/05/08 2010/08/27 MEDICIS Prescription
SOLODYN 050808 007 NDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 80MG BASE Yes No 2006/05/08 2010/08/27 MEDICIS Prescription
SOLODYN 050808 008 NDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 55MG BASE Yes No 2006/05/08 2010/08/27 MEDICIS Prescription
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