药品注册申请号:071935
申请类型:ANDA (仿制药申请)
申请人:AMNEAL PHARMS NY
申请人全名:AMNEAL PHARMACEUTICALS NY LLC
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 IBUPROFEN IBUPROFEN TABLET;ORAL 800MG No No AB 1987/10/13 1987/10/13 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
2024/11/21 SUPPL-36(补充) Approval Labeling STANDARD
2021/04/28 SUPPL-34(补充) Approval Labeling STANDARD
2019/07/22 SUPPL-33(补充) Approval Labeling STANDARD
2016/05/09 SUPPL-31(补充) Approval Labeling STANDARD
2007/12/26 SUPPL-27(补充) Approval Labeling
2006/08/07 SUPPL-23(补充) Approval Labeling
2006/07/03 SUPPL-22(补充) Approval Labeling
2001/09/25 SUPPL-17(补充) Approval Manufacturing (CMC)
2000/04/12 SUPPL-16(补充) Approval Manufacturing (CMC)
2000/04/12 SUPPL-15(补充) Approval Manufacturing (CMC)
2000/04/12 SUPPL-13(补充) Approval Manufacturing (CMC)
1999/09/24 SUPPL-11(补充) Approval Manufacturing (CMC)
1999/08/30 SUPPL-14(补充) Approval Labeling
1999/02/11 SUPPL-10(补充) Approval Manufacturing (CMC)
1998/01/20 SUPPL-8(补充) Approval Manufacturing (CMC)
1997/07/24 SUPPL-9(补充) Approval Manufacturing (CMC)
1992/01/30 SUPPL-7(补充) Approval Labeling
1988/06/30 SUPPL-4(补充) Approval Manufacturing (CMC)
1988/03/28 SUPPL-3(补充) Approval Labeling
1988/02/17 SUPPL-2(补充) Approval Manufacturing (CMC)
1988/02/17 SUPPL-1(补充) Approval Manufacturing (CMC)
1987/10/13 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:IBUPROFEN 剂型/给药途径:TABLET;ORAL 规格:800MG 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
072300 001 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB -- CONTRACT PHARMACAL
071935 001 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB 1987/10/13 AMNEAL PHARMS NY
071268 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB 1988/07/01 CONTRACT PHARMACAL
076112 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB 2001/10/31 DR REDDYS LABS INC
075682 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No Yes AB 2001/11/14 DR REDDYS
077114 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Discontinued No No AB 2005/07/18 L PERRIGO CO
078558 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB 2007/06/18 AMNEAL PHARMS NY
078329 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB 2009/02/05 STRIDES PHARMA
090796 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB 2010/12/21 MARKSANS PHARMA
091625 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB 2015/09/15 GRANULES
202413 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB 2016/11/23 SHANDONG XINHUA
213794 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB 2020/05/08 AUROBINDO PHARMA LTD
214699 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB 2021/09/13 ALKEM LABS LTD
215318 003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 800MG Prescription No No AB 2022/03/30 YICHANG HUMANWELL
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