药品注册申请号:216876
申请类型:ANDA (仿制药申请)
申请人:RUBICON
申请人全名:RUBICON RESEARCH PRIVATE LTD
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 LOPERAMIDE HYDROCHLORIDE LOPERAMIDE HYDROCHLORIDE CAPSULE;ORAL 2MG No No AB 2023/01/26 2023/01/26 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
2023/01/26 ORIG-1(原始申请) Approval STANDARD
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:LOPERAMIDE HYDROCHLORIDE 剂型/给药途径:CAPSULE;ORAL 规格:2MG 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
072741 001 ANDA LOPERAMIDE HYDROCHLORIDE LOPERAMIDE HYDROCHLORIDE CAPSULE;ORAL 2MG Prescription No Yes AB 1991/09/18 MYLAN
073192 001 ANDA LOPERAMIDE HYDROCHLORIDE LOPERAMIDE HYDROCHLORIDE CAPSULE;ORAL 2MG Prescription No No AB 1992/04/30 TEVA
215001 001 ANDA LOPERAMIDE HYDROCHLORIDE LOPERAMIDE HYDROCHLORIDE CAPSULE;ORAL 2MG Prescription No No AB 2021/10/06 EDENBRIDGE PHARMS
215579 001 ANDA LOPERAMIDE HYDROCHLORIDE LOPERAMIDE HYDROCHLORIDE CAPSULE;ORAL 2MG Prescription No No AB 2021/10/22 BIONPHARMA
216876 001 ANDA LOPERAMIDE HYDROCHLORIDE LOPERAMIDE HYDROCHLORIDE CAPSULE;ORAL 2MG Prescription No No AB 2023/01/26 RUBICON
217471 001 ANDA LOPERAMIDE HYDROCHLORIDE LOPERAMIDE HYDROCHLORIDE CAPSULE;ORAL 2MG Prescription No No AB 2023/03/23 ZYDUS LIFESCIENCES
217840 001 ANDA LOPERAMIDE HYDROCHLORIDE LOPERAMIDE HYDROCHLORIDE CAPSULE;ORAL 2MG Prescription No No AB 2023/07/05 JUBILANT CADISTA
218122 001 ANDA LOPERAMIDE HYDROCHLORIDE LOPERAMIDE HYDROCHLORIDE CAPSULE;ORAL 2MG Prescription No No AB 2023/09/05 AUROBINDO PHARMA LTD
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