药品注册申请号:078504
申请类型:ANDA (仿制药申请)
申请人:NORTHSTAR HLTHCARE
申请人全名:--
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 BACLOFEN BACLOFEN TABLET;ORAL 10MG No No AB 2009/09/18 -- Prescription
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
2015/04/15 SUPPL-5(补充) Approval Labeling STANDARD
2015/04/15 SUPPL-4(补充) Approval Labeling
2011/12/28 SUPPL-2(补充) Approval Labeling
2010/03/25 SUPPL-1(补充) Approval Labeling
2009/09/18 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
活性成分:BACLOFEN 剂型/给药途径:TABLET;ORAL 规格:10MG 治疗等效代码:AB
申请号产品号申请类型商品名活性成分剂型/给药途径规格市场状态RLDRSTE Code产品号批准日期申请人
077089 001 BACLOFEN BACLOFEN TABLET;ORAL 10MG Prescription No No AB --
078504 001 ANDA BACLOFEN BACLOFEN TABLET;ORAL 10MG Prescription No No AB -- NORTHSTAR HLTHCARE
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074584 001 ANDA BACLOFEN BACLOFEN TABLET;ORAL 10MG Prescription No No AB 1996/08/19 UPSHER SMITH LABS
077068 002 ANDA BACLOFEN BACLOFEN TABLET;ORAL 10MG Prescription No No AB 2005/08/30 ENDO OPERATIONS
077241 002 ANDA BACLOFEN BACLOFEN TABLET;ORAL 10MG Prescription No No AB 2007/07/06 LANNETT CO INC
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078401 002 ANDA BACLOFEN BACLOFEN TABLET;ORAL 10MG Prescription No No AB 2009/09/18 NORTHSTAR HLTHCARE
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214114 001 ANDA BACLOFEN BACLOFEN TABLET;ORAL 10MG Prescription No No AB 2021/07/16 BEXIMCO PHARMS USA
215885 002 ANDA BACLOFEN BACLOFEN TABLET;ORAL 10MG Prescription No No AB 2022/01/25 MANKIND PHARMA
217687 002 ANDA BACLOFEN BACLOFEN TABLET;ORAL 10MG Prescription No No AB 2023/11/08 MICRO LABS
217788 001 ANDA BACLOFEN BACLOFEN TABLET;ORAL 10MG Prescription No No AB 2024/01/10 GRAVITI PHARMS
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药品NDC数据与药品包装、标签说明书
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