药品注册申请号:019891
申请类型:NDA (新药申请)
申请人:RHODES PHARMS
申请人全名:RHODES PHARMACEUTICALS LP
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 DILAUDID HYDROMORPHONE HYDROCHLORIDE SOLUTION;ORAL 5MG/5ML Yes Yes AA 1992/12/07 1992/12/07 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
2023/12/15 SUPPL-31(补充) Approval Labeling STANDARD
2021/03/04 SUPPL-29(补充) Approval Labeling STANDARD
2019/10/07 SUPPL-28(补充) Approval Labeling STANDARD
2018/09/18 SUPPL-27(补充) Approval Labeling STANDARD
2018/09/18 SUPPL-26(补充) Approval REMS N/A
2016/12/16 SUPPL-24(补充) Approval Labeling STANDARD
2016/02/12 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
2016/02/12 SUPPL-21(补充) Approval Manufacturing (CMC) STANDARD
2016/02/05 SUPPL-23(补充) Approval Manufacturing (CMC) STANDARD
2015/03/09 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
2015/02/16 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
2013/11/14 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
2006/06/12 SUPPL-8(补充) Approval Labeling STANDARD
2003/03/10 SUPPL-2(补充) Approval Labeling STANDARD
2001/08/22 SUPPL-4(补充) Approval Labeling STANDARD
1999/11/24 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1995/03/31 SUPPL-1(补充) Approval Labeling STANDARD
1992/12/07 ORIG-1(原始申请) Approval Type 3 - New Dosage Form 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
001 6589960 2020/11/09 Y PDF格式**本条是由Drugfuture回溯的历史信息**
6589960 2020/11/09 Y Y PDF格式**本条是由Drugfuture回溯的历史信息**
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:HYDROMORPHONE HYDROCHLORIDE 剂型/给药途径:SOLUTION;ORAL 规格:5MG/5ML 治疗等效代码:AA
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
019891 001 NDA DILAUDID HYDROMORPHONE HYDROCHLORIDE SOLUTION;ORAL 5MG/5ML Prescription Yes Yes AA 1992/12/07 RHODES PHARMS
074653 001 ANDA HYDROMORPHONE HYDROCHLORIDE HYDROMORPHONE HYDROCHLORIDE SOLUTION;ORAL 5MG/5ML Prescription No No AA 1998/07/29 HIKMA
210176 001 ANDA HYDROMORPHONE HYDROCHLORIDE HYDROMORPHONE HYDROCHLORIDE SOLUTION;ORAL 5MG/5ML Prescription No No AA 2017/10/27 ASCENT PHARMS INC
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