药品注册申请号:076421
申请类型:ANDA (仿制药申请)
申请人:SUN PHARM INDS LTD
申请人全名:SUN PHARMACEUTICAL INDUSTRIES 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 FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 50MG No No AB 2003/03/28 2003/03/28 Prescription
002 FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 100MG No No AB 2003/03/28 Prescription
003 FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 150MG No No AB 2003/03/28 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
2003/03/28 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:FLECAINIDE ACETATE 剂型/给药途径:TABLET;ORAL 规格:50MG 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
075442 001 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 50MG Prescription No No AB 2001/07/31 AMNEAL PHARM
075882 001 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 50MG Prescription No No AB 2002/10/28 ANI PHARMS
076278 001 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 50MG Prescription No No AB 2003/01/14 HIKMA
076421 001 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 50MG Prescription No No AB 2003/03/28 SUN PHARM INDS LTD
202821 001 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 50MG Prescription No No AB 2017/11/03 AUROBINDO PHARMA LTD
210683 001 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 50MG Prescription No No AB 2020/09/16 BEXIMCO PHARMS USA
215599 001 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 50MG Prescription No No AB 2022/09/08 YICHANG HUMANWELL
活性成分:FLECAINIDE ACETATE 剂型/给药途径:TABLET;ORAL 规格:100MG 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
075442 002 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 100MG Prescription No No AB 2001/07/31 AMNEAL PHARM
075882 002 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 100MG Prescription No No AB 2002/10/28 ANI PHARMS
076278 002 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 100MG Prescription No No AB 2003/01/14 HIKMA
076421 002 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 100MG Prescription No No AB 2003/03/28 SUN PHARM INDS LTD
202821 002 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 100MG Prescription No No AB 2017/11/03 AUROBINDO PHARMA LTD
210683 002 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 100MG Prescription No No AB 2020/09/16 BEXIMCO PHARMS USA
215599 002 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 100MG Prescription No No AB 2022/09/08 YICHANG HUMANWELL
活性成分:FLECAINIDE ACETATE 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
075442 003 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 150MG Prescription No No AB 2001/07/31 AMNEAL PHARM
075882 003 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 150MG Prescription No No AB 2002/10/28 ANI PHARMS
076278 003 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 150MG Prescription No Yes AB 2003/01/14 HIKMA
076421 003 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 150MG Prescription No No AB 2003/03/28 SUN PHARM INDS LTD
202821 003 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 150MG Prescription No No AB 2017/11/03 AUROBINDO PHARMA LTD
210683 003 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 150MG Prescription No No AB 2020/09/16 BEXIMCO PHARMS USA
215599 003 ANDA FLECAINIDE ACETATE FLECAINIDE ACETATE TABLET;ORAL 150MG Prescription No No AB 2022/09/08 YICHANG HUMANWELL
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