药品注册申请号:202961
申请类型:ANDA (仿制药申请)
申请人:AMNEAL PHARMS
申请人全名:AMNEAL PHARMACEUTICALS
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 OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML No No AB 2012/09/17 2012/09/17 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
2012/09/17 ORIG-1(原始申请) Approval
>>>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
2025/02/07 SUPPL-20(补充) Approval Labeling-Package Insert STANDARD
2023/03/01 SUPPL-16(补充) Approval Labeling-Package Insert UNKNOWN
2022/11/01 SUPPL-6(补充) Approval Labeling-Package Insert,Labeling-Medication Guide STANDARD
2022/11/01 SUPPL-5(补充) Approval Labeling-Patient Package Insert,Labeling-Package Insert,Labeling-Medication Guide,Labeling-Container/Carton Labels STANDARD
2022/11/01 SUPPL-4(补充) Approval Labeling-Package Insert,Labeling-Medication Guide STANDARD
2015/02/04 SUPPL-2(补充) Approval Labeling-Package Insert STANDARD
2015/02/04 SUPPL-1(补充) Approval Labeling-Package Insert 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:OXCARBAZEPINE; 剂型/给药途径:SUSPENSION;ORAL; 规格:300MG/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
021285 001 NDA TRILEPTAL OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription Yes Yes AB 2001/05/25 NOVARTIS
078734 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription No No AB 2009/06/26 SUN PHARM INDS LTD
202961 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription No No AB 2012/09/17 AMNEAL PHARMS
201193 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Discontinued No No AB 2012/10/03 HIKMA
212428 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription No No AB 2021/06/21 CHARTWELL RX
211420 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Discontinued No No AB 2021/07/09 PAI HOLDINGS
215726 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription No No AB 2022/08/30 RUBICON RESEARCH
209652 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription No No AB 2022/11/04 BIONPHARMA
215332 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription No No AB 2022/11/30 AUCTA
213183 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription No No AB 2023/03/18 ALKEM LABS LTD
216749 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription No No AB 2023/10/20 HETERO LABS LTD III
217782 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription No No AB 2024/02/14 KANCHAN HLTHCARE
218278 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription No No AB 2024/03/01 BIOCON PHARMA
207300 001 ANDA OXCARBAZEPINE OXCARBAZEPINE SUSPENSION;ORAL 300MG/5ML Prescription No No AB 2025/07/11 MACLEODS PHARMS LTD
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药品NDC数据与药品包装、标签说明书
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