药品注册申请号:214739
申请类型:ANDA (仿制药申请)
申请人:EUGIA PHARMA
申请人全名:EUGIA PHARMA SPECIALITIES 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 BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 25MG/VIAL No No AP 2023/06/05 2023/06/05 Prescription
002 BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 100MG/VIAL No No AP 2023/06/05 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
2023/06/05 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:BENDAMUSTINE HYDROCHLORIDE 剂型/给药途径:POWDER;INTRAVENOUS 规格:25MG/VIAL 治疗等效代码:AP
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
022249 002 NDA TREANDA BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 25MG/VIAL Prescription Yes Yes AP 2009/05/01 CEPHALON
205376 001 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 25MG/VIAL Prescription No No AP 2022/12/07 DR REDDYS
205574 001 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 25MG/VIAL Prescription No No AP 2022/12/07 ACCORD HLTHCARE
205447 001 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 25MG/VIAL Discontinued No No AP 2023/02/14 BRECKENRIDGE
204104 001 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 25MG/VIAL Discontinued No No AP 2023/04/28 NORVIUM BIOSCIENCE
204230 001 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 25MG/VIAL Prescription No No AP 2023/06/05 APOTEX
211001 001 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 25MG/VIAL Prescription No No AP 2023/06/05 MEITHEAL
214739 001 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 25MG/VIAL Prescription No No AP 2023/06/05 EUGIA PHARMA
活性成分:BENDAMUSTINE HYDROCHLORIDE 剂型/给药途径:POWDER;INTRAVENOUS 规格:100MG/VIAL 治疗等效代码:AP
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
022249 001 NDA TREANDA BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 100MG/VIAL Prescription Yes Yes AP 2008/03/20 CEPHALON
205376 002 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 100MG/VIAL Prescription No No AP 2022/12/07 DR REDDYS
205574 002 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 100MG/VIAL Prescription No No AP 2022/12/07 ACCORD HLTHCARE
205447 002 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 100MG/VIAL Discontinued No No AP 2023/02/14 BRECKENRIDGE
204104 002 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 100MG/VIAL Discontinued No No AP 2023/04/28 NORVIUM BIOSCIENCE
204230 002 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 100MG/VIAL Prescription No No AP 2023/06/05 APOTEX
211001 002 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 100MG/VIAL Prescription No No AP 2023/06/05 MEITHEAL
214739 002 ANDA BENDAMUSTINE HYDROCHLORIDE BENDAMUSTINE HYDROCHLORIDE POWDER;INTRAVENOUS 100MG/VIAL Prescription No No AP 2023/06/05 EUGIA PHARMA
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