药品注册申请号:200534
申请类型:NDA (新药申请)
申请人:GENUS LIFESCIENCES
申请人全名:GENUS LIFE SCIENCES 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 OXYCODONE HYDROCHLORIDE OXYCODONE HYDROCHLORIDE CAPSULE;ORAL 5MG Yes Yes AB 2010/10/20 2010/10/20 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
2024/04/19 SUPPL-14(补充) Approval Labeling STANDARD
2023/12/15 SUPPL-13(补充) Approval Labeling STANDARD
2021/07/21 SUPPL-10(补充) Approval Efficacy STANDARD
2021/03/04 SUPPL-11(补充) Approval Labeling STANDARD
2019/10/07 SUPPL-9(补充) Approval Labeling STANDARD
2018/09/18 SUPPL-8(补充) Approval Labeling STANDARD
2018/09/18 SUPPL-7(补充) Approval REMS N/A
2016/12/16 SUPPL-6(补充) Approval Labeling STANDARD
2015/11/16 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
2014/06/02 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
2010/10/20 ORIG-1(原始申请) Approval Type 7 - Drug Already Marketed without Approved NDA 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
001 M-14 2024/07/21
与本品治疗等效的药品
活性成分:OXYCODONE HYDROCHLORIDE 剂型/给药途径:CAPSULE;ORAL 规格:5MG 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
200534 001 NDA OXYCODONE HYDROCHLORIDE OXYCODONE HYDROCHLORIDE CAPSULE;ORAL 5MG Prescription Yes Yes AB 2010/10/20 GENUS LIFESCIENCES
203107 001 ANDA OXYCODONE HYDROCHLORIDE OXYCODONE HYDROCHLORIDE CAPSULE;ORAL 5MG Discontinued No No AB 2012/07/26 DR REDDYS LABS SA
202773 001 ANDA OXYCODONE HYDROCHLORIDE OXYCODONE HYDROCHLORIDE CAPSULE;ORAL 5MG Prescription No No AB 2015/08/17 AVANTHI INC
204752 001 ANDA OXYCODONE HYDROCHLORIDE OXYCODONE HYDROCHLORIDE CAPSULE;ORAL 5MG Prescription No No AB 2015/08/24 NOVEL LABS INC
205177 001 ANDA OXYCODONE HYDROCHLORIDE OXYCODONE HYDROCHLORIDE CAPSULE;ORAL 5MG Prescription No No AB 2016/03/31 ANI PHARMS
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