药品注册申请号:077852
申请类型:ANDA (仿制药申请)
申请人:HIKMA
申请人全名:HIKMA PHARMACEUTICALS USA INC
产品信息
产品号商品名活性成分剂型/给药途径规格/剂量参比药物(RLD)生物等效参考标准(RS)治疗等效代码该申请号批准日期该产品号批准日期市场状态
001 ROPINIROLE HYDROCHLORIDE ROPINIROLE HYDROCHLORIDE TABLET;ORAL EQ 0.25MG BASE No No None 2008/05/05 2008/05/05 Discontinued
002 ROPINIROLE HYDROCHLORIDE ROPINIROLE HYDROCHLORIDE TABLET;ORAL EQ 0.5MG BASE No No None 2008/05/05 Discontinued
003 ROPINIROLE HYDROCHLORIDE ROPINIROLE HYDROCHLORIDE TABLET;ORAL EQ 1MG BASE No No None 2008/05/05 Discontinued
004 ROPINIROLE HYDROCHLORIDE ROPINIROLE HYDROCHLORIDE TABLET;ORAL EQ 2MG BASE No No None 2008/05/05 Discontinued
005 ROPINIROLE HYDROCHLORIDE ROPINIROLE HYDROCHLORIDE TABLET;ORAL EQ 3MG BASE No No None 2008/05/05 Discontinued
006 ROPINIROLE HYDROCHLORIDE ROPINIROLE HYDROCHLORIDE TABLET;ORAL EQ 4MG BASE No No None 2008/05/05 Discontinued
007 ROPINIROLE HYDROCHLORIDE ROPINIROLE HYDROCHLORIDE TABLET;ORAL EQ 5MG BASE No No None 2008/05/19 Discontinued
批准日期,申请提交历史,通知信,药品说明书,审评文件等信息
提交状态日期提交号审批结论申请内容分类审评优先级;罕用药状态通知信、审评文件、说明书、包装标签备注
2021/03/26 SUPPL-11(补充) Approval Labeling STANDARD
2021/03/26 SUPPL-9(补充) Approval Labeling STANDARD
2015/10/19 SUPPL-8(补充) Approval Labeling STANDARD
2012/09/07 SUPPL-6(补充) Approval Labeling
2011/08/15 SUPPL-4(补充) Approval Labeling
2009/11/17 SUPPL-3(补充) Approval Labeling
2008/05/21 SUPPL-2(补充) Approval Labeling
2008/05/05 ORIG-1(原始申请) Approval
与本品相关的专利信息(来自FDA橙皮书Orange Book)
关联产品号专利号专利过期日是否物质专利是否产品专利专利用途代码撤销请求提交日期专利下载备注
与本品相关的市场独占权保护信息
关联产品号独占权代码失效日期备注
与本品治疗等效的药品
本品无治疗等效药品
更多信息
药品NDC数据与药品包装、标签说明书
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