药品注册申请号:070145
申请类型:ANDA (仿制药申请)
申请人:MYLAN PHARMS INC
申请人全名:MYLAN PHARMACEUTICALS 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 PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE TABLET;ORAL 650MG;100MG No No None 1986/06/12 1985/06/12 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
2002/01/04 SUPPL-31(补充) Approval Manufacturing (CMC)
2002/01/04 SUPPL-30(补充) Approval Manufacturing (CMC)
2002/01/04 SUPPL-29(补充) Approval Manufacturing (CMC)
2000/10/13 SUPPL-27(补充) Approval Manufacturing (CMC)
2000/09/21 SUPPL-33(补充) Approval Labeling
2000/08/14 SUPPL-26(补充) Approval Manufacturing (CMC)
2000/08/14 SUPPL-25(补充) Approval Manufacturing (CMC)
2000/05/02 SUPPL-28(补充) Approval Labeling
1998/02/25 SUPPL-24(补充) Approval Manufacturing (CMC)
1998/02/05 SUPPL-23(补充) Approval Manufacturing (CMC)
1996/08/07 SUPPL-22(补充) Approval Manufacturing (CMC)
1996/04/19 SUPPL-21(补充) Approval Manufacturing (CMC)
1996/04/19 SUPPL-20(补充) Approval Manufacturing (CMC)
1993/12/22 SUPPL-19(补充) Approval Manufacturing (CMC)
1991/10/31 SUPPL-16(补充) Approval Labeling
1991/10/31 SUPPL-9(补充) Approval Manufacturing (CMC)
1990/07/18 SUPPL-15(补充) Approval Manufacturing (CMC)
1990/04/02 SUPPL-11(补充) Approval Labeling
1989/07/31 SUPPL-14(补充) Approval Manufacturing (CMC)
1989/07/31 SUPPL-13(补充) Approval Manufacturing (CMC)
1988/10/20 SUPPL-10(补充) Approval Manufacturing (CMC)
1987/01/09 SUPPL-6(补充) Approval Manufacturing (CMC)
1987/01/09 SUPPL-5(补充) Approval Manufacturing (CMC)
1987/01/09 SUPPL-4(补充) Approval Manufacturing (CMC)
1986/06/12 ORIG-1(原始申请) Approval
1985/12/30 SUPPL-2(补充) Approval Manufacturing (CMC)
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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