药品注册申请号：211623
申请类型：ANDA (仿制药申请)
申请人：UNIQUE PHARM
申请人全名：UNIQUE PHARMACEUTICAL LABORATORIES
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 CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG No No AB 2020/04/24 2020/04/24 Prescription
002 CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG No No AB 2020/04/24 Prescription
003 CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG No No AB 2020/04/24 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
2024/01/29 SUPPL-4（补充） Approval Labeling STANDARD
2020/04/24 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
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:CARBAMAZEPINE 剂型/给药途径:TABLET, EXTENDED RELEASE;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
020234 001 NDA TEGRETOL-XR CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription Yes No AB 1996/03/25 NOVARTIS
078115 001 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription No No AB 2009/03/31 TARO
205571 001 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription No No AB 2019/02/07 ZYDUS PHARMS
211623 001 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription No No AB 2020/04/24 UNIQUE PHARM
213311 001 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription No No AB 2021/04/13 CSPC OUYI
212948 001 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription No No AB 2021/09/30 ANBISON LAB
215591 001 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription No No AB 2022/03/31 ZHEJIANG JIUZHOU
216594 001 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription No No AB 2022/08/18 UMEDICA
216404 001 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription No No AB 2022/12/02 RICONPHARMA LLC
216235 001 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription No No AB 2023/03/02 SCIECURE PHARMA INC
212704 001 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Discontinued No No AB 2023/09/22 AMNEAL PHARMS
213159 001 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription No No AB 2024/03/08 APOTEX
活性成分:CARBAMAZEPINE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:200MG 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
020234 002 NDA TEGRETOL-XR CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription Yes No AB 1996/03/25 NOVARTIS
078115 002 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription No No AB 2009/03/31 TARO
205571 002 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription No No AB 2019/02/07 ZYDUS PHARMS
211623 002 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription No No AB 2020/04/24 UNIQUE PHARM
213311 002 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription No No AB 2021/04/13 CSPC OUYI
212948 002 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription No No AB 2021/09/30 ANBISON LAB
215591 002 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription No No AB 2022/03/31 ZHEJIANG JIUZHOU
216594 002 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription No No AB 2022/08/18 UMEDICA
216404 002 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription No No AB 2022/12/02 RICONPHARMA LLC
216235 002 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription No No AB 2023/03/02 SCIECURE PHARMA INC
212704 002 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Discontinued No No AB 2023/09/22 AMNEAL PHARMS
213159 002 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription No No AB 2024/03/08 APOTEX
活性成分:CARBAMAZEPINE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:400MG 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
020234 003 NDA TEGRETOL-XR CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription Yes Yes AB 1996/03/25 NOVARTIS
078115 003 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2009/03/31 TARO
205571 003 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2019/02/07 ZYDUS PHARMS
211623 003 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2020/04/24 UNIQUE PHARM
213311 003 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2021/04/13 CSPC OUYI
212948 003 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2021/09/30 ANBISON LAB
215591 003 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2022/03/31 ZHEJIANG JIUZHOU
216594 003 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2022/08/18 UMEDICA
216404 003 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2022/12/02 RICONPHARMA LLC
216235 003 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2023/03/02 SCIECURE PHARMA INC
212704 003 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Discontinued No No AB 2023/09/22 AMNEAL PHARMS
213159 003 ANDA CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2024/03/08 APOTEX
更多信息
药品NDC数据与药品包装、标签说明书
参考引用1
参考引用2
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