药品注册申请号:216400
申请类型:ANDA (仿制药申请)
申请人:ALKEM LABS LTD
申请人全名:ALKEM LABORATORIES LTD
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 FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML No No AB 2023/05/15 2023/05/15 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
>>>原始批准或临时批准<<<
审批日期提交号审批结论提交分类审评优先级;罕用药状态通知信、审评文件、说明书、包装标签备注
2023/05/15 ORIG-1(原始申请) Approval STANDARD
>>>补充申请<<<
审批日期提交号审批结论补充类别或审批类型审评优先级;罕用药状态通知信、审评文件、说明书、包装标签备注
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:FAMOTIDINE; 剂型/给药途径:FOR SUSPENSION;ORAL; 规格:40MG/5ML; 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
091020 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2010/05/27 NAVINTA LLC
090440 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2010/06/29 LUPIN LTD
201695 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2012/12/17 NOVEL LABS INC
201995 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2014/05/30 NOVITIUM PHARMA
215043 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No Yes AB 2021/04/20 NOVITIUM PHARMA
216427 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2022/08/04 AMNEAL
216400 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2023/05/15 ALKEM LABS LTD
217655 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2023/06/16 APPCO
217137 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2023/07/07 PHARMOBEDIENT
217330 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2023/08/17 ANNORA PHARMA
217842 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2023/09/14 MICRO LABS
217529 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2023/09/18 AJANTA PHARMA LTD
217605 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2024/01/16 UNICHEM
218344 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2024/10/16 EPIC PHARMA LLC
217982 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2025/06/02 LANNETT CO INC
219153 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Discontinued No No AB 2025/06/23 BIONPHARMA
219091 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2025/07/09 AUROBINDO PHARMA LTD
219863 001 ANDA FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML Prescription No No AB 2025/07/24 MSN
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