药品注册申请号:011011
申请类型:NDA (新药申请)
申请人:AUXILIUM PHARMS LLC
申请人全名:AUXILIUM PHARMACEUTICALS 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
004 ROBAXIN METHOCARBAMOL TABLET;ORAL 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None 1957/07/16 Approved Prior to Jan 1, 1982 Discontinued
006 ROBAXIN-750 METHOCARBAMOL TABLET;ORAL 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None Approved Prior to Jan 1, 1982 Discontinued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
2019/03/01 SUPPL-79(补充) Approval Labeling STANDARD
2015/03/09 SUPPL-77(补充) Approval Manufacturing (CMC) STANDARD
2003/05/01 SUPPL-71(补充) Approval Labeling STANDARD
2003/05/01 SUPPL-70(补充) Approval Labeling STANDARD
1998/04/22 SUPPL-69(补充) Approval Manufacturing (CMC) STANDARD
1990/08/21 SUPPL-66(补充) Approval Manufacturing (CMC) STANDARD
1989/01/06 SUPPL-64(补充) Approval Manufacturing (CMC) STANDARD
1987/01/28 SUPPL-63(补充) Approval Manufacturing (CMC) STANDARD
1986/04/16 SUPPL-62(补充) Approval Manufacturing (CMC) STANDARD
1986/04/16 SUPPL-61(补充) Approval Manufacturing (CMC) STANDARD
1985/10/25 SUPPL-60(补充) Approval Labeling
1985/04/29 SUPPL-59(补充) Approval Manufacturing (CMC) STANDARD
1985/04/29 SUPPL-58(补充) Approval Manufacturing (CMC) STANDARD
1984/06/27 SUPPL-57(补充) Approval Manufacturing (CMC) STANDARD
1983/04/07 SUPPL-54(补充) Approval Manufacturing (CMC) STANDARD
1983/01/25 SUPPL-55(补充) Approval Manufacturing (CMC) STANDARD
1982/10/18 SUPPL-53(补充) Approval Manufacturing (CMC) STANDARD
1982/10/01 SUPPL-52(补充) Approval Manufacturing (CMC) STANDARD
1982/07/15 SUPPL-42(补充) Approval Manufacturing (CMC) STANDARD
1982/03/15 SUPPL-49(补充) Approval Manufacturing (CMC) STANDARD
1982/01/18 SUPPL-50(补充) Approval Manufacturing (CMC) STANDARD
1982/01/18 SUPPL-44(补充) Approval Manufacturing (CMC) STANDARD
1981/12/24 SUPPL-47(补充) Approval Manufacturing (CMC) STANDARD
1981/12/24 SUPPL-46(补充) Approval Manufacturing (CMC) STANDARD
1981/12/21 SUPPL-48(补充) Approval Manufacturing (CMC) STANDARD
1981/12/07 SUPPL-39(补充) Approval Labeling
1981/11/02 SUPPL-43(补充) Approval Manufacturing (CMC) STANDARD
1981/10/28 SUPPL-38(补充) Approval Labeling
1981/01/22 SUPPL-41(补充) Approval Manufacturing (CMC) STANDARD
1981/01/22 SUPPL-40(补充) Approval Manufacturing (CMC) STANDARD
1980/02/11 SUPPL-32(补充) Approval Manufacturing (CMC) STANDARD
1979/07/24 SUPPL-31(补充) Approval Manufacturing (CMC) STANDARD
1979/05/21 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
1979/05/21 SUPPL-20(补充) Approval Labeling
1979/05/21 SUPPL-19(补充) Approval Labeling
1976/03/10 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1975/05/01 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1975/04/29 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1975/04/29 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1974/12/09 SUPPL-11(补充) Approval Labeling
1974/10/22 SUPPL-15(补充) Approval Labeling
1974/10/17 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1957/07/16 ORIG-1(原始申请) Approval Type 1 - New Molecular Entity 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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