药品名称 | UNIPEN | 申请号 | 050320 | 产品号 | 001 | 活性成分 | NAFCILLIN SODIUM | 市场状态 | 停止上市 | 剂型或给药途径 | INJECTABLE;INJECTION | 规格 | EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | 治疗等效代码 | | 参比药物 | 否 | 批准日期 | Approved Prior to Jan 1, 1982 | 申请机构 | WYETH AYERST LABORATORIES
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与本品相关的专利信息(来自橙皮书Orange Book) | 专利号 | 专利过期日 | 是否化合物专利 | 是否产品专利 | 专利用途代码 | 专利下载 | 无 | 历史专利信息 | 无 |
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与本品相关的市场独占权保护信息 | 独占权代码 | 失效日期 | 无 | 历史市场独占权保护信息 | 无 |
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与药品注册相关的信息 | 申请号 | 修订号 | 审批结论 | 公开文档类型 | 文档创建时间 | 获取文档 | 无 |
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药品注册审批历史信息 | 申请号 | 修订号 | 审批结论 | 审批日期 | 审批内容 | 050320 | 070 | AP | 1982/08/12 | Labeling Revision | 050320 | 069 | AP | 1982/05/12 | Labeling Revision | 050320 | 068 | AP | 1981/06/01 | Labeling Revision | 050320 | 067 | AP | 1981/06/01 | Control Supplement | 050320 | 066 | AP | 1981/04/08 | Labeling Revision | 050320 | 065 | AP | 1981/04/08 | Control Supplement | 050320 | 064 | AP | 1980/11/21 | Labeling Revision | 050320 | 063 | AP | 1980/08/20 | Expiration Date Change | 050320 | 062 | AP | 1979/07/30 | Labeling Revision | 050320 | 061 | AP | 1979/02/23 | Labeling Revision | 050320 | 060 | AP | 1979/02/23 | Labeling Revision | 050320 | 059 | AP | 1978/12/21 | Labeling Revision | 050320 | 058 | AP | 1978/12/21 | Control Supplement | 050320 | 057 | AP | 1978/04/28 | Labeling Revision | 050320 | 056 | AP | 1978/02/06 | Labeling Revision | 050320 | 055 | AP | 1977/12/22 | Labeling Revision | 050320 | 054 | AP | 1977/10/04 | Labeling Revision | 050320 | 053 | AP | 1978/01/19 | Expiration Date Change | 050320 | 052 | AP | 1978/01/19 | Expiration Date Change | 050320 | 051 | AP | 1977/08/10 | Labeling Revision | 050320 | 050 | AP | 1977/06/01 | Control Supplement | 050320 | 049 | AP | 1977/02/11 | Labeling Revision | 050320 | 047 | AP | 1977/06/20 | Control Supplement | 050320 | 046 | AP | 1977/01/11 | Labeling Revision | 050320 | 045 | AP | 1977/01/11 | Labeling Revision | 050320 | 044 | AP | 1976/09/23 | Labeling Revision | 050320 | 043 | AP | 1976/09/07 | Labeling Revision | 050320 | 042 | AP | 1976/09/07 | Control Supplement | 050320 | 041 | AP | 1976/03/23 | Labeling Revision | 050320 | 040 | AP | 1976/03/23 | Labeling Revision | 050320 | 039 | AP | 1976/03/23 | Labeling Revision | 050320 | 038 | AP | 1976/02/13 | Labeling Revision | 050320 | 036 | AP | 1975/05/22 | Labeling Revision | 050320 | 035 | AP | 1975/08/19 | Labeling Revision | 050320 | 034 | AP | 1975/01/23 | Labeling Revision | 050320 | 031 | AP | 1974/08/02 | Labeling Revision | 050320 | 030 | AP | 1974/03/12 | Labeling Revision | 050320 | 029 | AP | 1974/01/24 | Labeling Revision | 050320 | 028 | AP | 1973/11/23 | Labeling Revision | 050320 | 027 | AP | 1973/11/19 | Labeling Revision | 050320 | 024 | AP | 1972/01/11 | Labeling Revision | 050320 | 023 | AP | 1971/12/06 | Labeling Revision | 050320 | 022 | AP | 1971/10/22 | Labeling Revision | 050320 | 021 | AP | 1971/09/24 | Control Supplement | 050320 | 020 | AP | 1972/08/31 | Labeling Revision | 050320 | 019 | AP | 1971/05/19 | Labeling Revision | 050320 | 018 | AP | 1971/05/18 | Labeling Revision | 050320 | 017 | AP | 1971/04/02 | Labeling Revision | 050320 | 016 | AP | 1970/12/11 | Labeling Revision | 050320 | 015 | AP | 1970/08/10 | Labeling Revision | 050320 | 012 | AP | 1988/08/31 | Control Supplement | 050320 | 011 | AP | 1988/07/20 | Labeling Revision | 050320 | 010 | AP | 1988/12/19 | Control Supplement | 050320 | 009 | AP | 1988/02/22 | Labeling Revision | 050320 | 008 | AP | 1987/07/08 | Labeling Revision | 050320 | 007 | AP | 1987/04/14 | Control Supplement | 050320 | 006 | AP | 1985/08/27 | Labeling Revision | 050320 | 005 | AP | 1987/07/29 | Control Supplement | 050320 | 004 | AP | 1986/12/02 | Manufacturing Change or Addition | 050320 | 003 | AP | 1985/12/03 | Control Supplement | 050320 | 002 | AP | 1983/01/19 | Control Supplement | 050320 | 001 | AP | 1982/12/28 | Labeling Revision | 050320 | 000 | AP | 1970/06/23 | Approval |
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