药品注册申请号:017122
申请类型:NDA (新药申请)
申请人:XANODYNE PHARM
申请人全名:XANODYNE PHARMACEUTICS 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 DARVOCET-N 50 ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE TABLET;ORAL 325MG;50MG No No None 1972/12/19 Approved Prior to Jan 1, 1982 Discontinued
002 DARVOCET-N 100 ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE TABLET;ORAL 650MG;100MG No No None Approved Prior to Jan 1, 1982 Discontinued
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
2009/09/25 SUPPL-62(补充) Approval Labeling STANDARD
2009/09/25 SUPPL-61(补充) Approval Labeling STANDARD
2007/01/24 SUPPL-59(补充) Approval Manufacturing (CMC) STANDARD
2006/05/11 SUPPL-58(补充) Approval Manufacturing (CMC) STANDARD
2005/07/13 SUPPL-57(补充) Approval Manufacturing (CMC) STANDARD
2005/04/12 SUPPL-56(补充) Approval Manufacturing (CMC) STANDARD
2005/02/03 SUPPL-55(补充) Approval Manufacturing (CMC) STANDARD
2005/02/03 SUPPL-54(补充) Approval Manufacturing (CMC) STANDARD
2001/10/30 SUPPL-47(补充) Approval Labeling STANDARD
2001/10/30 SUPPL-46(补充) Approval Labeling STANDARD
1999/02/24 SUPPL-53(补充) Approval Manufacturing (CMC) STANDARD
1998/10/05 SUPPL-52(补充) Approval Manufacturing (CMC) STANDARD
1998/08/10 SUPPL-51(补充) Approval Manufacturing (CMC) STANDARD
1998/04/02 SUPPL-50(补充) Approval Manufacturing (CMC) STANDARD
1997/05/15 SUPPL-48(补充) Approval Manufacturing (CMC) STANDARD
1995/03/20 SUPPL-39(补充) Approval Labeling STANDARD
1995/03/14 SUPPL-45(补充) Approval Manufacturing (CMC) STANDARD
1994/09/02 SUPPL-43(补充) Approval Labeling STANDARD
1994/08/23 SUPPL-40(补充) Approval Labeling STANDARD
1994/04/05 SUPPL-44(补充) Approval Manufacturing (CMC) STANDARD
1993/12/17 SUPPL-41(补充) Approval Manufacturing (CMC) STANDARD
1992/09/15 SUPPL-42(补充) Approval Manufacturing (CMC) STANDARD
1987/04/16 SUPPL-34(补充) Approval Manufacturing (CMC) STANDARD
1986/10/17 SUPPL-30(补充) Approval Labeling STANDARD
1986/04/21 SUPPL-29(补充) Approval Labeling STANDARD
1986/04/03 SUPPL-28(补充) Approval Labeling STANDARD
1984/08/16 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
1984/08/07 SUPPL-24(补充) Approval Labeling STANDARD
1981/10/28 SUPPL-23(补充) Approval Labeling STANDARD
1981/05/20 SUPPL-22(补充) Approval Labeling STANDARD
1980/04/16 SUPPL-21(补充) Approval Labeling STANDARD
1980/01/21 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1979/11/06 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1979/09/26 SUPPL-20(补充) Approval Labeling STANDARD
1979/07/17 SUPPL-18(补充) Approval Labeling STANDARD
1979/06/29 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1978/10/16 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1977/06/10 SUPPL-11(补充) Approval Labeling STANDARD
1977/05/06 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1977/05/06 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1976/09/15 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1974/06/18 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1972/12/19 ORIG-1(原始申请) Approval Type 4 - New Combination STANDARD
与本品相关的专利信息(来自FDA橙皮书Orange Book)
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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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