药品注册申请号:076550
申请类型:ANDA (仿制药申请)
申请人:ANI PHARMS
申请人全名:ANI PHARMACEUTICALS 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 PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 150MG No No AB 2004/04/23 2004/04/23 Prescription
002 PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 225MG No No AB 2004/04/23 Prescription
003 PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 300MG No No AB 2004/04/23 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
2019/10/30 SUPPL-11(补充) Approval Labeling STANDARD
2004/04/23 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:PROPAFENONE HYDROCHLORIDE 剂型/给药途径:TABLET;ORAL 规格:150MG 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
075203 001 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 150MG Prescription No No AB 2000/10/24 WATSON LABS
075998 001 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 150MG Discontinued No No AB 2001/11/29 SUN PHARM INDUSTRIES
075938 001 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 150MG Prescription No No AB 2002/10/17 STRIDES PHARMA
076550 001 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 150MG Prescription No No AB 2004/04/23 ANI PHARMS
202445 001 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 150MG Prescription No No AB 2016/05/11 AUROBINDO PHARMA
活性成分:PROPAFENONE HYDROCHLORIDE 剂型/给药途径:TABLET;ORAL 规格:225MG 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
075203 002 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 225MG Prescription No No AB 2000/10/24 WATSON LABS
075998 002 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 225MG Discontinued No No AB 2001/11/29 SUN PHARM INDUSTRIES
075938 002 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 225MG Prescription No No AB 2002/10/17 STRIDES PHARMA
076550 002 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 225MG Prescription No No AB 2004/04/23 ANI PHARMS
202445 002 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 225MG Prescription No No AB 2016/05/11 AUROBINDO PHARMA
活性成分:PROPAFENONE HYDROCHLORIDE 剂型/给药途径:TABLET;ORAL 规格:300MG 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
075998 003 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 300MG Discontinued No No AB 2001/11/29 SUN PHARM INDUSTRIES
075938 003 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 300MG Prescription No Yes AB 2002/10/17 STRIDES PHARMA
076550 003 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 300MG Prescription No No AB 2004/04/23 ANI PHARMS
202445 003 ANDA PROPAFENONE HYDROCHLORIDE PROPAFENONE HYDROCHLORIDE TABLET;ORAL 300MG Prescription No No AB 2016/05/11 AUROBINDO PHARMA
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