药品注册申请号:075977
申请类型:ANDA (仿制药申请)
申请人:TEVA
申请人全名:TEVA PHARMACEUTICALS USA 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 TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG No No AB 2002/06/19 2002/06/19 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
2024/03/22 SUPPL-29(补充) Approval Manufacturing (CMC) UNKNOWN
2023/12/18 SUPPL-32(补充) Approval Labeling STANDARD
2023/12/18 SUPPL-31(补充) Approval Labeling STANDARD
2023/12/07 SUPPL-28(补充) Approval Labeling STANDARD
2023/12/07 SUPPL-26(补充) Approval Labeling STANDARD
2023/12/07 SUPPL-23(补充) Approval Labeling STANDARD
2023/12/07 SUPPL-20(补充) Approval Labeling STANDARD
2023/12/07 SUPPL-19(补充) Approval Labeling STANDARD
2023/12/07 SUPPL-16(补充) Approval Labeling STANDARD
2023/12/07 SUPPL-15(补充) Approval Labeling STANDARD
2018/09/18 SUPPL-17(补充) Approval REMS
2015/11/09 SUPPL-11(补充) Approval Labeling STANDARD
2010/11/22 SUPPL-5(补充) Approval Labeling
2005/04/08 SUPPL-3(补充) Approval Labeling
2002/10/30 SUPPL-1(补充) Approval Labeling
2002/06/19 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:TRAMADOL HYDROCHLORIDE 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
075964 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No Yes AB 2002/06/19 SUN PHARM INDS INC
075977 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No No AB 2002/06/19 TEVA
076003 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No No AB 2002/06/20 AMNEAL PHARMS
075986 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Discontinued No No AB 2002/06/21 MYLAN
075981 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No No AB 2002/07/10 APOTEX
090404 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No No AB 2011/01/31 ZYDUS PHARMS USA INC
202075 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No No AB 2011/11/28 ACI
201973 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No No AB 2012/11/16 IPCA LABS LTD
091498 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No No AB 2013/03/29 CSPC OUYI PHARM CO
203494 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No No AB 2014/03/31 AUROBINDO PHARMA LTD
208708 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No No AB 2019/06/28 RUBICON
206706 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No No AB 2019/07/02 MERRO PHARM USA
211825 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET;ORAL 50MG Prescription No No AB 2019/08/09 UNICHEM
更多信息
药品NDC数据与药品包装、标签说明书
©2006-2024 DrugFuture->U.S. FDA Drugs Database