药品注册申请号：021151
申请类型：NDA (新药申请)
申请人：LEGACY PHARMA
申请人全名：LEGACY PHARMA 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 BETAPACE AF SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Yes No AB 2000/02/22 2000/02/22 Prescription
002 BETAPACE AF SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Yes No AB 2000/02/22 Prescription
003 BETAPACE AF SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Yes Yes AB 2000/02/22 Prescription
005 BETAPACE AF SOTALOL HYDROCHLORIDE TABLET;ORAL 100MG No No None 2003/03/14 Discontinued
006 BETAPACE AF SOTALOL HYDROCHLORIDE TABLET;ORAL 40MG No No None 2003/04/02 Discontinued
007 BETAPACE AF SOTALOL HYDROCHLORIDE TABLET;ORAL 60MG No No None 2003/04/02 Discontinued
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
2011/08/17 SUPPL-10（补充） Approval Labeling UNKNOWN
2011/02/03 SUPPL-9（补充） Approval Labeling UNKNOWN
2003/04/02 SUPPL-5（补充） Approval Manufacturing (CMC) STANDARD
2003/03/14 SUPPL-4（补充） Approval Manufacturing (CMC) STANDARD
2001/10/01 SUPPL-3（补充） Approval Labeling STANDARD
2000/11/22 SUPPL-1（补充） Approval Manufacturing (CMC) STANDARD ;Orphan
2000/02/22 ORIG-1（原始申请） Approval Type 6 - New Indication (no longer used) STANDARD ;Orphan
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
无
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
无
与本品治疗等效的药品
活性成分:SOTALOL HYDROCHLORIDE 剂型/给药途径:TABLET;ORAL 规格:80MG 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
019865 001 NDA BETAPACE SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Prescription Yes No AB 1992/10/30 LEGACY PHARMA
021151 001 NDA BETAPACE AF SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Prescription Yes No AB 2000/02/22 LEGACY PHARMA
075429 001 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Prescription No No AB 2000/05/01 TEVA
075500 001 ANDA SORINE SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Prescription No No AB 2001/04/27 AIPING PHARM INC
076140 001 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Prescription No No AB 2002/09/26 APOTEX
076214 001 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Prescription No No AB 2003/08/27 APOTEX
075563 001 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Prescription No No AB 2003/11/07 OXFORD PHARMS
077070 001 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Prescription No No AB 2005/11/04 EPIC PHARMA LLC
077616 001 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Prescription No No AB 2007/02/07 AUROBINDO PHARMA USA
207428 001 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Prescription No No AB 2016/10/21 BEXIMCO PHARMS USA
207429 001 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 80MG Prescription No No AB 2018/11/02 BEXIMCO PHARMS USA
活性成分:SOTALOL HYDROCHLORIDE 剂型/给药途径:TABLET;ORAL 规格:120MG 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
019865 005 NDA BETAPACE SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Prescription Yes No AB 1994/04/20 LEGACY PHARMA
021151 002 NDA BETAPACE AF SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Prescription Yes No AB 2000/02/22 LEGACY PHARMA
075429 002 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Prescription No No AB 2000/05/01 TEVA
075500 004 ANDA SORINE SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Prescription No No AB 2001/04/27 AIPING PHARM INC
076140 002 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Prescription No No AB 2002/09/26 APOTEX
076214 002 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Prescription No No AB 2003/08/27 APOTEX
075563 002 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Prescription No No AB 2003/11/07 OXFORD PHARMS
077070 002 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Prescription No No AB 2005/11/04 EPIC PHARMA LLC
077616 002 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Prescription No No AB 2007/02/07 AUROBINDO PHARMA USA
207428 002 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Prescription No No AB 2016/10/21 BEXIMCO PHARMS USA
207429 002 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 120MG Prescription No No AB 2018/11/02 BEXIMCO PHARMS USA
活性成分:SOTALOL HYDROCHLORIDE 剂型/给药途径:TABLET;ORAL 规格:160MG 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
019865 002 NDA BETAPACE SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Prescription Yes Yes AB 1992/10/30 LEGACY PHARMA
021151 003 NDA BETAPACE AF SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Prescription Yes Yes AB 2000/02/22 LEGACY PHARMA
075429 003 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Prescription No No AB 2000/05/01 TEVA
075500 002 ANDA SORINE SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Prescription No No AB 2001/04/27 AIPING PHARM INC
076140 003 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Prescription No No AB 2002/09/26 APOTEX
076214 003 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Prescription No No AB 2003/08/27 APOTEX
075563 003 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Prescription No No AB 2003/11/07 OXFORD PHARMS
077070 003 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Prescription No No AB 2005/11/04 EPIC PHARMA LLC
077616 003 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Prescription No No AB 2007/02/07 AUROBINDO PHARMA USA
207428 003 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Prescription No No AB 2016/10/21 BEXIMCO PHARMS USA
207429 003 ANDA SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET;ORAL 160MG Prescription No No AB 2018/11/02 BEXIMCO PHARMS USA
更多信息
药品NDC数据与药品包装、标签说明书
参考引用1
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