药品注册申请号:079040
申请类型:ANDA (仿制药申请)
申请人:ACTAVIS ELIZABETH
申请人全名:ACTAVIS ELIZABETH LLC AN INDIRECT WHOLLY OWNED SUB OF TEVA PHARMACEUTICALS USA INC
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 MORPHINE SULFATE MORPHINE SULFATE CAPSULE, EXTENDED RELEASE;ORAL 30MG No No None 2013/01/16 2013/01/16 Prescription
002 MORPHINE SULFATE MORPHINE SULFATE CAPSULE, EXTENDED RELEASE;ORAL 45MG No No None 2013/01/16 Prescription
003 MORPHINE SULFATE MORPHINE SULFATE CAPSULE, EXTENDED RELEASE;ORAL 60MG No No None 2013/01/16 Prescription
004 MORPHINE SULFATE MORPHINE SULFATE CAPSULE, EXTENDED RELEASE;ORAL 75MG No No None 2013/01/16 Prescription
005 MORPHINE SULFATE MORPHINE SULFATE CAPSULE, EXTENDED RELEASE;ORAL 90MG No No None 2013/01/16 Prescription
006 MORPHINE SULFATE MORPHINE SULFATE CAPSULE, EXTENDED RELEASE;ORAL 120MG No Yes None 2013/01/16 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
2024/10/31 SUPPL-30(补充) Approval REMS
2023/12/15 SUPPL-27(补充) Approval Labeling STANDARD
2023/12/15 SUPPL-26(补充) Approval Labeling STANDARD
2023/12/04 SUPPL-24(补充) Approval Labeling STANDARD
2021/03/11 SUPPL-15(补充) Approval Labeling STANDARD
2021/03/11 SUPPL-13(补充) Approval Labeling STANDARD
2021/03/04 SUPPL-23(补充) Approval Labeling STANDARD
2021/02/02 SUPPL-20(补充) Approval Labeling STANDARD
2019/10/11 SUPPL-21(补充) Approval Labeling STANDARD
2018/09/18 SUPPL-18(补充) Approval REMS
2017/05/26 SUPPL-17(补充) Approval REMS
2016/09/30 SUPPL-14(补充) Approval REMS
2016/04/20 SUPPL-11(补充) Approval REMS
2015/06/26 SUPPL-10(补充) Approval REMS
2014/08/19 SUPPL-7(补充) Approval REMS
2014/07/03 SUPPL-5(补充) Approval Labeling STANDARD
2014/07/02 SUPPL-4(补充) Approval Manufacturing (CMC) UNKNOWN
2013/04/15 SUPPL-3(补充) Approval REMS
2013/01/16 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
本品无治疗等效药品
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