药品注册申请号:089025
申请类型:ANDA (仿制药申请)
申请人:TEVA
申请人全名: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 PROPOXYPHENE COMPOUND 65 ASPIRIN; CAFFEINE; PROPOXYPHENE HYDROCHLORIDE CAPSULE;ORAL 389MG;32.4MG;65MG No No None 1985/03/29 1985/03/29 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
2002/11/14 SUPPL-42(补充) Approval Manufacturing (CMC)
2001/12/20 SUPPL-41(补充) Approval Manufacturing (CMC)
2001/12/20 SUPPL-40(补充) Approval Manufacturing (CMC)
2000/07/07 SUPPL-39(补充) Approval Manufacturing (CMC)
1998/08/26 SUPPL-38(补充) Approval Manufacturing (CMC)
1998/03/09 SUPPL-37(补充) Approval Manufacturing (CMC)
1998/03/06 SUPPL-36(补充) Approval Labeling
1997/06/02 SUPPL-35(补充) Approval Manufacturing (CMC)
1997/03/19 SUPPL-34(补充) Approval Manufacturing (CMC)
1996/11/04 SUPPL-33(补充) Approval Manufacturing (CMC)
1996/08/16 SUPPL-32(补充) Approval Labeling
1996/01/25 SUPPL-31(补充) Approval Manufacturing (CMC)
1996/01/25 SUPPL-30(补充) Approval Manufacturing (CMC)
1996/01/25 SUPPL-29(补充) Approval Manufacturing (CMC)
1995/03/02 SUPPL-28(补充) Approval Manufacturing (CMC)
1994/11/03 SUPPL-7(补充) Approval Manufacturing (CMC)
1994/03/15 SUPPL-20(补充) Approval Manufacturing (CMC)
1994/01/26 SUPPL-27(补充) Approval Manufacturing (CMC)
1994/01/26 SUPPL-26(补充) Approval Manufacturing (CMC)
1994/01/26 SUPPL-25(补充) Approval Manufacturing (CMC)
1994/01/26 SUPPL-24(补充) Approval Manufacturing (CMC)
1994/01/26 SUPPL-23(补充) Approval Manufacturing (CMC)
1994/01/26 SUPPL-22(补充) Approval Manufacturing (CMC)
1993/07/30 SUPPL-21(补充) Approval Manufacturing (CMC)
1993/07/30 SUPPL-14(补充) Approval Manufacturing (CMC)
1993/05/25 SUPPL-19(补充) Approval Manufacturing (CMC)
1993/05/25 SUPPL-18(补充) Approval Manufacturing (CMC)
1993/05/25 SUPPL-17(补充) Approval Manufacturing (CMC)
1993/05/25 SUPPL-13(补充) Approval Manufacturing (CMC)
1993/05/25 SUPPL-12(补充) Approval Manufacturing (CMC)
1993/04/01 SUPPL-16(补充) Approval Manufacturing (CMC)
1993/04/01 SUPPL-15(补充) Approval Manufacturing (CMC)
1993/04/01 SUPPL-11(补充) Approval Manufacturing (CMC)
1990/10/11 SUPPL-10(补充) Approval Bioequivalence
1989/07/11 SUPPL-6(补充) Approval Labeling
1989/04/17 SUPPL-4(补充) Approval Manufacturing (CMC)
1989/04/17 SUPPL-3(补充) Approval Manufacturing (CMC)
1989/04/17 SUPPL-2(补充) Approval Manufacturing (CMC)
1989/02/08 SUPPL-5(补充) Approval Labeling
1985/03/29 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)
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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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