药品注册申请号:205257
申请类型:ANDA (仿制药申请)
申请人:MYLAN
申请人全名:MYLAN PHARMACEUTICALS 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, EXTENDED RELEASE;ORAL 100MG No No AB1 2015/12/22 2015/12/22 Discontinued
002 TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 200MG No No AB1 2015/12/22 Discontinued
003 TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 300MG No No AB1 2015/12/22 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
2024/10/31 SUPPL-13(补充) Approval REMS
2023/12/15 SUPPL-11(补充) Approval Labeling STANDARD
2021/09/10 SUPPL-10(补充) Approval Labeling STANDARD
2021/03/04 SUPPL-9(补充) Approval Labeling STANDARD
2019/10/11 SUPPL-8(补充) Approval Labeling STANDARD
2018/09/21 SUPPL-7(补充) Approval Labeling STANDARD
2018/09/18 SUPPL-6(补充) Approval REMS
2018/08/24 SUPPL-5(补充) Approval Labeling STANDARD
2017/08/29 SUPPL-4(补充) Approval Labeling STANDARD
2017/08/21 SUPPL-3(补充) Approval Labeling STANDARD
2015/12/22 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
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, EXTENDED RELEASE;ORAL 规格:100MG 治疗等效代码:AB1
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
200503 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 100MG Prescription No Yes AB1 2011/08/29 LUPIN LTD
201384 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 100MG Discontinued No No AB1 2011/12/07 SUN PHARM
205257 001 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 100MG Discontinued No No AB1 2015/12/22 MYLAN
活性成分:TRAMADOL HYDROCHLORIDE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:200MG 治疗等效代码:AB1
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
200503 002 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 200MG Prescription No No AB1 2011/08/29 LUPIN LTD
201384 002 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 200MG Discontinued No No AB1 2011/12/07 SUN PHARM
205257 002 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 200MG Discontinued No No AB1 2015/12/22 MYLAN
活性成分:TRAMADOL HYDROCHLORIDE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:300MG 治疗等效代码:AB1
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
200503 003 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 300MG Prescription No No AB1 2011/08/29 LUPIN LTD
201384 003 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 300MG Discontinued No No AB1 2011/12/07 SUN PHARM
205257 003 ANDA TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 300MG Discontinued No No AB1 2015/12/22 MYLAN
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