药品注册申请号:074501
申请类型:ANDA (仿制药申请)
申请人:SANDOZ
申请人全名:SANDOZ 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 NADOLOL NADOLOL TABLET;ORAL 20MG No No AB 1995/11/09 1995/11/09 Prescription
002 NADOLOL NADOLOL TABLET;ORAL 40MG No No AB 1995/11/09 Prescription
003 NADOLOL NADOLOL TABLET;ORAL 80MG No No AB 1995/11/09 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
2015/06/13 SUPPL-6(补充) Approval Labeling
2008/07/29 SUPPL-4(补充) Approval Labeling
2000/01/03 SUPPL-2(补充) Approval Manufacturing (CMC)
2000/01/03 SUPPL-1(补充) Approval Manufacturing (CMC)
1995/11/09 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:NADOLOL 剂型/给药途径:TABLET;ORAL 规格:20MG 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
018063 005 NDA CORGARD NADOLOL TABLET;ORAL 20MG Prescription Yes No AB 1986/10/28 USWM
074172 001 ANDA NADOLOL NADOLOL TABLET;ORAL 20MG Prescription No No AB 1993/10/31 RISING
074501 001 ANDA NADOLOL NADOLOL TABLET;ORAL 20MG Prescription No No AB 1995/11/09 SANDOZ
074229 001 ANDA NADOLOL NADOLOL TABLET;ORAL 20MG Discontinued No No AB 1996/08/30 HERITAGE PHARMA
203455 001 ANDA NADOLOL NADOLOL TABLET;ORAL 20MG Prescription No No AB 2015/12/18 INVAGEN PHARMS
208832 001 ANDA NADOLOL NADOLOL TABLET;ORAL 20MG Prescription No No AB 2017/06/02 AMNEAL PHARMS CO
207761 001 ANDA NADOLOL NADOLOL TABLET;ORAL 20MG Prescription No No AB 2017/07/28 ZYDUS PHARMS
209309 001 ANDA NADOLOL NADOLOL TABLET;ORAL 20MG Prescription No No AB 2017/10/05 CHARTWELL RX
210955 001 ANDA NADOLOL NADOLOL TABLET;ORAL 20MG Prescription No No AB 2018/07/23 BEXIMCO PHARMS USA
212856 001 ANDA NADOLOL NADOLOL TABLET;ORAL 20MG Prescription No No AB 2019/09/13 RK PHARMA
201893 003 ANDA NADOLOL NADOLOL TABLET;ORAL 20MG Prescription No No AB 2022/06/07 AUROBINDO PHARMA
211763 001 ANDA NADOLOL NADOLOL TABLET;ORAL 20MG Prescription No No AB 2023/06/02 ALEMBIC
活性成分:NADOLOL 剂型/给药途径:TABLET;ORAL 规格:40MG 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
018063 001 NDA CORGARD NADOLOL TABLET;ORAL 40MG Prescription Yes No AB Approved Prior to Jan 1, 1982 USWM
074172 002 ANDA NADOLOL NADOLOL TABLET;ORAL 40MG Prescription No No AB 1993/10/31 RISING
074501 002 ANDA NADOLOL NADOLOL TABLET;ORAL 40MG Prescription No No AB 1995/11/09 SANDOZ
074229 002 ANDA NADOLOL NADOLOL TABLET;ORAL 40MG Discontinued No No AB 1996/08/30 HERITAGE PHARMA
201893 001 ANDA NADOLOL NADOLOL TABLET;ORAL 40MG Prescription No No AB 2015/09/16 AUROBINDO PHARMA
203455 002 ANDA NADOLOL NADOLOL TABLET;ORAL 40MG Prescription No No AB 2015/12/18 INVAGEN PHARMS
208832 002 ANDA NADOLOL NADOLOL TABLET;ORAL 40MG Prescription No No AB 2017/06/02 AMNEAL PHARMS CO
207761 002 ANDA NADOLOL NADOLOL TABLET;ORAL 40MG Prescription No No AB 2017/07/28 ZYDUS PHARMS
209309 002 ANDA NADOLOL NADOLOL TABLET;ORAL 40MG Prescription No No AB 2017/10/05 CHARTWELL RX
210955 002 ANDA NADOLOL NADOLOL TABLET;ORAL 40MG Prescription No No AB 2018/07/23 BEXIMCO PHARMS USA
212856 002 ANDA NADOLOL NADOLOL TABLET;ORAL 40MG Prescription No No AB 2019/09/13 RK PHARMA
211763 002 ANDA NADOLOL NADOLOL TABLET;ORAL 40MG Prescription No No AB 2023/06/02 ALEMBIC
活性成分:NADOLOL 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
018063 002 NDA CORGARD NADOLOL TABLET;ORAL 80MG Prescription Yes Yes AB Approved Prior to Jan 1, 1982 USWM
074172 003 ANDA NADOLOL NADOLOL TABLET;ORAL 80MG Prescription No No AB 1993/10/31 RISING
074501 003 ANDA NADOLOL NADOLOL TABLET;ORAL 80MG Prescription No No AB 1995/11/09 SANDOZ
074255 001 ANDA NADOLOL NADOLOL TABLET;ORAL 80MG Discontinued No No AB 1996/01/24 HERITAGE PHARMA
201893 002 ANDA NADOLOL NADOLOL TABLET;ORAL 80MG Prescription No No AB 2015/09/16 AUROBINDO PHARMA
203455 003 ANDA NADOLOL NADOLOL TABLET;ORAL 80MG Prescription No No AB 2015/12/18 INVAGEN PHARMS
208832 003 ANDA NADOLOL NADOLOL TABLET;ORAL 80MG Prescription No No AB 2017/06/02 AMNEAL PHARMS CO
207761 003 ANDA NADOLOL NADOLOL TABLET;ORAL 80MG Prescription No No AB 2017/07/28 ZYDUS PHARMS
209309 003 ANDA NADOLOL NADOLOL TABLET;ORAL 80MG Prescription No No AB 2017/10/05 CHARTWELL RX
210955 003 ANDA NADOLOL NADOLOL TABLET;ORAL 80MG Prescription No No AB 2018/07/23 BEXIMCO PHARMS USA
212856 003 ANDA NADOLOL NADOLOL TABLET;ORAL 80MG Prescription No No AB 2019/09/13 RK PHARMA
211763 003 ANDA NADOLOL NADOLOL TABLET;ORAL 80MG Prescription No No AB 2023/06/02 ALEMBIC
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