药品注册申请号:018337
申请类型:NDA (新药申请)
申请人:TARO
申请人全名:TARO PHARMACEUTICAL INDUSTRIES LTD
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 ACETAMINOPHEN ACETAMINOPHEN SUPPOSITORY;RECTAL 650MG Yes Yes None 1980/04/22 Approved Prior to Jan 1, 1982 Over-the-counter
002 ACETAMINOPHEN ACETAMINOPHEN SUPPOSITORY;RECTAL 325MG Yes No None Approved Prior to Jan 1, 1982 Over-the-counter
003 ACETAMINOPHEN ACETAMINOPHEN SUPPOSITORY;RECTAL 120MG Yes No None 1983/09/12 Over-the-counter
004 INFANTS' FEVERALL ACETAMINOPHEN SUPPOSITORY;RECTAL 80MG Yes No None 1992/08/26 Over-the-counter
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
2020/02/07 SUPPL-35(补充) Approval Labeling STANDARD
2015/08/12 SUPPL-34(补充) Approval Labeling STANDARD
2015/01/05 SUPPL-33(补充) Approval Manufacturing (CMC) STANDARD
2014/01/16 SUPPL-32(补充) Approval Labeling STANDARD
2010/10/20 SUPPL-29(补充) Approval Labeling STANDARD
2010/04/05 SUPPL-28(补充) Approval Labeling STANDARD
2008/06/27 SUPPL-25(补充) Approval Manufacturing (CMC) N/A
2007/11/02 SUPPL-24(补充) Approval Manufacturing (CMC) N/A
2002/10/09 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
2000/09/21 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1994/06/15 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1993/01/28 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1992/08/26 SUPPL-13(补充) Approval Labeling
1988/06/08 SUPPL-8(补充) Approval Labeling
1980/04/22 ORIG-1(原始申请) Approval Type 5 - New Formulation or New Manufacturer STANDARD
与本品相关的专利信息(来自FDA橙皮书Orange Book)
关联产品号专利号专利过期日是否物质专利是否产品专利专利用途代码撤销请求提交日期专利下载备注
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
更多信息
药品NDC数据与药品包装、标签说明书
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