药品注册申请号:018965
申请类型:NDA (新药申请)
申请人:ATNAHS PHARMA US
申请人全名:ATNAHS PHARMA US 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 NAPROSYN NAPROXEN SUSPENSION;ORAL 25MG/ML Yes No AB 1987/03/23 1987/03/23 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-28(补充) Approval Labeling STANDARD
2021/04/28 SUPPL-27(补充) Approval Labeling STANDARD
2019/07/22 SUPPL-26(补充) Approval Labeling STANDARD
2017/03/10 SUPPL-25(补充) Approval Labeling STANDARD
2016/05/09 SUPPL-24(补充) Approval Manufacturing (CMC) PRIORITY
2016/05/09 SUPPL-23(补充) Approval Labeling STANDARD
2016/05/09 SUPPL-22(补充) Approval Labeling STANDARD
2015/07/30 SUPPL-21(补充) Approval Manufacturing (CMC) PRIORITY
2013/03/22 SUPPL-20(补充) Approval Labeling STANDARD
2008/07/25 SUPPL-18(补充) Approval Labeling STANDARD
2007/09/20 SUPPL-16(补充) Approval Labeling STANDARD
2007/04/19 SUPPL-15(补充) Approval Labeling STANDARD
2006/03/10 SUPPL-13(补充) Approval Labeling STANDARD
2006/01/24 SUPPL-14(补充) Approval Labeling STANDARD
2004/11/10 SUPPL-10(补充) Approval Labeling STANDARD
2004/11/10 SUPPL-9(补充) Approval Labeling STANDARD
2003/04/14 SUPPL-7(补充) Approval Labeling STANDARD
2002/02/22 SUPPL-12(补充) Approval Manufacturing (CMC) PRIORITY
2001/01/05 SUPPL-11(补充) Approval Manufacturing (CMC) PRIORITY
1996/11/14 SUPPL-8(补充) Approval Manufacturing (CMC) PRIORITY
1994/09/12 SUPPL-6(补充) Approval Manufacturing (CMC) PRIORITY
1993/01/27 SUPPL-4(补充) Approval Manufacturing (CMC) PRIORITY
1987/03/23 ORIG-1(原始申请) Approval Type 3 - New Dosage Form PRIORITY
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:NAPROXEN 剂型/给药途径:SUSPENSION;ORAL 规格:25MG/ML 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
018965 001 NDA NAPROSYN NAPROXEN SUSPENSION;ORAL 25MG/ML Prescription Yes No AB 1987/03/23 ATNAHS PHARMA US
074190 001 ANDA NAPROXEN NAPROXEN SUSPENSION;ORAL 25MG/ML Prescription No Yes AB 1994/03/30 HIKMA
212705 001 ANDA NAPROXEN NAPROXEN SUSPENSION;ORAL 25MG/ML Prescription No No AB 2020/07/31 AMNEAL
211910 001 ANDA NAPROXEN NAPROXEN SUSPENSION;ORAL 25MG/ML Prescription No No AB 2021/03/10 NOVITIUM PHARMA
215776 001 ANDA NAPROXEN NAPROXEN SUSPENSION;ORAL 25MG/ML Prescription No No AB 2022/06/07 HETERO LABS LTD III
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