药品注册申请号:017549
申请类型:NDA (新药申请)
申请人:MERIDIAN MEDCL TECHN
申请人全名:MERIDIAN MEDICAL TECHNOLOGIES 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 LIDOPEN LIDOCAINE HYDROCHLORIDE INJECTABLE;INJECTION 10% No No None 1975/03/28 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
2002/10/31 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
2000/10/20 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1999/12/08 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1998/07/21 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1997/04/18 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1997/01/09 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1996/06/06 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1993/05/10 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1988/12/23 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1986/12/10 SUPPL-11(补充) Approval Labeling
1984/04/16 SUPPL-8(补充) Approval Labeling
1978/01/11 SUPPL-7(补充) Approval Labeling
1977/03/17 SUPPL-4(补充) Approval Labeling
1976/10/18 SUPPL-3(补充) Approval Efficacy
1975/12/04 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
1975/09/24 SUPPL-1(补充) Approval Labeling
1975/03/28 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)
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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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