药品注册申请号:016891
申请类型:NDA (新药申请)
申请人:SANOFI AVENTIS US
申请人全名:SANOFI AVENTIS US 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
001 TALWIN COMPOUND ASPIRIN; PENTAZOCINE HYDROCHLORIDE TABLET;ORAL 325MG;EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None 1975/11/12 Approved Prior to Jan 1, 1982 Discontinued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
1996/07/25 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1995/11/29 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1991/01/03 SUPPL-18(补充) Approval Labeling STANDARD
1989/01/05 SUPPL-16(补充) Approval Labeling STANDARD
1989/01/05 SUPPL-15(补充) Approval Labeling STANDARD
1989/01/05 SUPPL-9(补充) Approval Labeling STANDARD
1988/03/17 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1982/03/09 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1981/12/01 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1981/10/02 SUPPL-11(补充) Approval Labeling STANDARD
1980/11/05 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1979/05/30 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1979/05/08 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1979/05/08 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1979/05/08 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1977/12/09 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1977/05/13 SUPPL-2(补充) Approval Labeling STANDARD
1976/02/23 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1975/11/12 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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药品NDC数据与药品包装、标签说明书
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