药品注册申请号:074278
申请类型:ANDA (仿制药申请)
申请人:HIKMA
申请人全名:HIKMA 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 LEVORPHANOL TARTRATE LEVORPHANOL TARTRATE TABLET;ORAL 2MG No No AB 2000/03/31 2000/03/31 Prescription
002 LEVORPHANOL TARTRATE LEVORPHANOL TARTRATE TABLET;ORAL 1MG No No None 2018/06/18 Discontinued
003 LEVORPHANOL TARTRATE LEVORPHANOL TARTRATE TABLET;ORAL 3MG No No AB 2018/06/18 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
2023/12/15 SUPPL-20(补充) Approval Labeling STANDARD
2021/03/04 SUPPL-17(补充) Approval Labeling STANDARD
2020/03/05 SUPPL-16(补充) Approval Labeling STANDARD
2019/10/11 SUPPL-14(补充) Approval Labeling STANDARD
2018/09/21 SUPPL-13(补充) Approval Labeling STANDARD
2018/09/18 SUPPL-12(补充) Approval REMS
2018/06/18 SUPPL-11(补充) Approval STANDARD
2016/12/16 SUPPL-9(补充) Approval Labeling STANDARD
2016/12/16 SUPPL-8(补充) Approval Labeling STANDARD
2008/07/16 SUPPL-5(补充) Approval Labeling
2005/04/08 SUPPL-3(补充) Approval Labeling
2000/09/05 SUPPL-1(补充) Approval Manufacturing (CMC)
2000/03/31 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:LEVORPHANOL TARTRATE 剂型/给药途径:TABLET;ORAL 规格:2MG 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
074278 001 ANDA LEVORPHANOL TARTRATE LEVORPHANOL TARTRATE TABLET;ORAL 2MG Prescription No No AB 2000/03/31 HIKMA
211484 001 ANDA LEVORPHANOL TARTRATE LEVORPHANOL TARTRATE TABLET;ORAL 2MG Prescription No No AB 2018/12/13 VIRTUS
212024 001 ANDA LEVORPHANOL TARTRATE LEVORPHANOL TARTRATE TABLET;ORAL 2MG Prescription No No AB 2019/12/13 SPECGX LLC
213479 001 ANDA LEVORPHANOL TARTRATE LEVORPHANOL TARTRATE TABLET;ORAL 2MG Prescription No No AB 2020/07/01 NOVITIUM PHARMA
213906 001 ANDA LEVORPHANOL TARTRATE LEVORPHANOL TARTRATE TABLET;ORAL 2MG Prescription No No AB 2021/06/17 SUN PHARM INDS INC
活性成分:LEVORPHANOL TARTRATE 剂型/给药途径:TABLET;ORAL 规格:3MG 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
074278 003 ANDA LEVORPHANOL TARTRATE LEVORPHANOL TARTRATE TABLET;ORAL 3MG Discontinued No No AB 2018/06/18 HIKMA
213479 002 ANDA LEVORPHANOL TARTRATE LEVORPHANOL TARTRATE TABLET;ORAL 3MG Prescription No Yes AB 2021/01/12 NOVITIUM PHARMA
213906 002 ANDA LEVORPHANOL TARTRATE LEVORPHANOL TARTRATE TABLET;ORAL 3MG Prescription No No AB 2023/04/25 SUN PHARM INDS INC
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