药品注册申请号:206329
申请类型:ANDA (仿制药申请)
申请人:DR REDDYS LABS SA
申请人全名:DR REDDYS LABORATORIES SA
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 FENTANYL CITRATE FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.1MG BASE No No AB 2022/08/22 2022/08/22 Discontinued
002 FENTANYL CITRATE FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.2MG BASE No No AB 2022/08/22 Discontinued
003 FENTANYL CITRATE FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.3MG BASE No No None 2022/08/22 Discontinued
004 FENTANYL CITRATE FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.4MG BASE No No AB 2022/08/22 Discontinued
005 FENTANYL CITRATE FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.6MG BASE No No AB 2022/08/22 Discontinued
006 FENTANYL CITRATE FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.8MG BASE No No AB 2022/08/22 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
2022/12/08 SUPPL-1(补充) Approval REMS
2022/08/22 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:FENTANYL CITRATE 剂型/给药途径:TABLET;BUCCAL, SUBLINGUAL 规格:EQ 0.1MG BASE 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
021947 001 NDA FENTORA FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.1MG BASE Discontinued Yes No AB 2006/09/25 CEPHALON
206329 001 ANDA FENTANYL CITRATE FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.1MG BASE Discontinued No No AB 2022/08/22 DR REDDYS LABS SA
活性成分:FENTANYL CITRATE 剂型/给药途径:TABLET;BUCCAL, SUBLINGUAL 规格:EQ 0.2MG BASE 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
021947 002 NDA FENTORA FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.2MG BASE Discontinued Yes No AB 2006/09/25 CEPHALON
206329 002 ANDA FENTANYL CITRATE FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.2MG BASE Discontinued No No AB 2022/08/22 DR REDDYS LABS SA
活性成分:FENTANYL CITRATE 剂型/给药途径:TABLET;BUCCAL, SUBLINGUAL 规格:EQ 0.4MG BASE 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
021947 003 NDA FENTORA FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.4MG BASE Discontinued Yes No AB 2006/09/25 CEPHALON
206329 004 ANDA FENTANYL CITRATE FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.4MG BASE Discontinued No No AB 2022/08/22 DR REDDYS LABS SA
活性成分:FENTANYL CITRATE 剂型/给药途径:TABLET;BUCCAL, SUBLINGUAL 规格:EQ 0.6MG BASE 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
021947 004 NDA FENTORA FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.6MG BASE Discontinued Yes No AB 2006/09/25 CEPHALON
206329 005 ANDA FENTANYL CITRATE FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.6MG BASE Discontinued No No AB 2022/08/22 DR REDDYS LABS SA
活性成分:FENTANYL CITRATE 剂型/给药途径:TABLET;BUCCAL, SUBLINGUAL 规格:EQ 0.8MG BASE 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
021947 005 NDA FENTORA FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.8MG BASE Discontinued Yes No AB 2006/09/25 CEPHALON
206329 006 ANDA FENTANYL CITRATE FENTANYL CITRATE TABLET;BUCCAL, SUBLINGUAL EQ 0.8MG BASE Discontinued No No AB 2022/08/22 DR REDDYS LABS SA
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