药品名称 | FOCALIN XR | 申请号 | 021802 | 产品号 | 004 | 活性成分 | DEXMETHYLPHENIDATE HYDROCHLORIDE | 市场状态 | 处方药 | 剂型或给药途径 | CAPSULE, EXTENDED RELEASE;ORAL | 规格 | 15MG | 治疗等效代码 | AB | 参比药物 | 否 | 批准日期 | 2006/08/01 | 申请机构 | NOVARTIS PHARMACEUTICALS CORP
| 化学类型 | New dosage form | 审评分类 | Standard review drug |
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与本品相关的市场独占权保护信息 | 独占权代码 | 失效日期 | 无 | 历史市场独占权保护信息 | M-74 | 2009/04/11 | M-80 | 2011/10/17 | NDF | 2008/05/26 |
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与药品注册相关的信息 | 申请号 | 修订号 | 审批结论 | 公开文档类型 | 文档创建时间 | 获取文档 | 021802 | 028 | AP | Letter | 2015/04/20 | 下载 | 021802 | 028 | AP | Label | 2015/04/21 | 下载 | 021802 | 026 | AP | Letter | 2013/12/13 | 下载 | 021802 | 026 | AP | Label | 2013/12/17 | 下载 | 021802 | 025 | AP | Letter | 2013/06/12 | 下载 | 021802 | 025 | AP | Label | 2013/06/18 | 下载 | 021802 | 024 | AP | Letter | 2012/05/04 | 下载 | 021802 | 024 | AP | Label | 2012/05/07 | 下载 | 021802 | 022 | AP | Label | 2011/11/29 | 下载 | 021802 | 021 | AP | Label | 2010/11/19 | 下载 | 021802 | 021 | AP | Letter | 2010/11/22 | 下载 | 021802 | 017 | AP | Letter | 2010/05/07 | 下载 | 021802 | 017 | AP | Label | 2010/05/07 | 下载 | 021802 | 016 | AP | Label | 2009/10/30 | 下载 | 021802 | 016 | AP | Letter | 2009/12/11 | 下载 | 021802 | 014 | AP | Letter | 2009/12/11 | 下载 | 021802 | 014 | AP | Label | 2009/10/30 | 下载 | 021802 | 012 | AP | Letter | 2008/10/22 | 下载 | 021802 | 009 | AP | Label | 2007/05/01 | 下载 | 021802 | 009 | AP | Letter | 2007/05/01 | 下载 | 021802 | 007 | AP | Letter | 2006/08/04 | 下载 | 021802 | 007 | AP | Label | 2006/08/04 | 下载 | 021802 | 005 | AP | Letter | 2006/04/13 | 下载 | 021802 | 005 | AP | Label | 2006/04/12 | 下载 | 021802 | 003 | AP | Label | 2006/08/04 | 下载 | 021802 | 003 | AP | Letter | 2006/08/04 | 下载 | 021802 | 001 | AP | Letter | 2006/04/13 | 下载 | 021802 | 001 | AP | Label | 2006/04/12 | 下载 | 021802 | 000 | AP | Other Important Information from FDA | 2007/05/10 | 下载 | 021802 | 000 | AP | Review | 2007/07/02 | 下载 | 021802 | 000 | AP | Letter | 2005/06/07 | 下载 | 021802 | 000 | AP | Label | 2005/06/07 | 下载 | 021802 | 000 | AP | Medication Guide | 2009/10/30 | 下载 |
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药品注册审批历史信息 | 申请号 | 修订号 | 审批结论 | 审批日期 | 审批内容 | 021802 | 031 | AP | 2015/12/04 | Manufacturing Change or Addition | 021802 | 028 | AP | 2015/04/17 | Labeling Revision | 021802 | 027 | AP | 2015/06/12 | Manufacturing Change or Addition | 021802 | 026 | AP | 2013/12/12 | Labeling Revision | 021802 | 025 | AP | 2013/06/11 | Labeling Revision | 021802 | 024 | AP | 2012/05/02 | Labeling Revision | 021802 | 022 | AP | 2011/04/21 | Manufacturing Change or Addition | 021802 | 021 | AP | 2010/11/15 | Labeling Revision | 021802 | 017 | AP | 2010/05/04 | Labeling Revision | 021802 | 016 | AP | 2009/10/23 | Labeling Revision | 021802 | 014 | AP | 2009/10/23 | New Dosage Regimen | 021802 | 012 | AP | 2008/10/17 | Labeling Revision | 021802 | 009 | AP | 2007/04/25 | Labeling Revision | 021802 | 007 | AP | 2006/08/01 | Control Supplement | 021802 | 005 | AP | 2006/04/11 | Labeling Revision | 021802 | 003 | AP | 2006/08/01 | Labeling Revision | 021802 | 001 | AP | 2006/04/11 | Efficacy Supplement with Clinical Data to Support | 021802 | 000 | AP | 2005/05/26 | Approval |
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