| 药品名称 | DIAMOX | | 申请号 | 008943 | 产品号 | 002 | | 活性成分 | ACETAZOLAMIDE | 市场状态 | 停止上市 | | 剂型或给药途径 | TABLET;ORAL | 规格 | 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | | 治疗等效代码 | | 参比药物 | 否 | | 批准日期 | Approved Prior to Jan 1, 1982 | 申请机构 | TEVA BRANDED PHARMACEUTICAL PRODUCTS R AND D INC
| | 化学类型 | New molecular entity (NME) | 审评分类 | Priority review drug |
|
|
| 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 |
|
| 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 |
|
| 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 |
|
| 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 | | 008943 | 048 | AP | 1999/01/05 | Package Change | | 008943 | 047 | AP | 1991/02/14 | Control Supplement | | 008943 | 046 | AP | 1990/11/28 | Labeling Revision | | 008943 | 045 | AP | 1990/04/23 | Control Supplement | | 008943 | 044 | AP | 1990/01/24 | Labeling Revision | | 008943 | 043 | AP | 1989/12/06 | Labeling Revision | | 008943 | 042 | AP | 1988/07/21 | Expiration Date Change | | 008943 | 041 | AP | 1988/06/22 | Labeling Revision | | 008943 | 040 | AP | 1987/08/11 | Labeling Revision | | 008943 | 039 | AP | 1987/06/16 | Control Supplement | | 008943 | 038 | AP | 1987/10/06 | Control Supplement | | 008943 | 037 | AP | 1987/03/03 | Labeling Revision | | 008943 | 036 | AP | 1986/03/21 | Labeling Revision | | 008943 | 035 | AP | 1985/05/13 | Labeling Revision | | 008943 | 034 | AP | 1984/09/25 | Control Supplement | | 008943 | 033 | AP | 1984/02/22 | Formulation Revision | | 008943 | 032 | AP | 1982/09/29 | Control Supplement | | 008943 | 031 | AP | 1982/04/02 | Package Change | | 008943 | 030 | AP | 1981/06/12 | Formulation Revision | | 008943 | 029 | AP | 1980/12/17 | Formulation Revision | | 008943 | 028 | AP | 1980/12/17 | Formulation Revision | | 008943 | 027 | AP | 1980/12/17 | Control Supplement | | 008943 | 026 | AP | 1979/08/30 | Formulation Revision | | 008943 | 025 | AP | 1984/02/14 | Control Supplement | | 008943 | 024 | AP | 1979/07/31 | Control Supplement | | 008943 | 023 | AP | 1978/10/02 | Labeling Revision | | 008943 | 022 | AP | 1978/04/07 | Control Supplement | | 008943 | 021 | AP | 1978/04/03 | Formulation Revision | | 008943 | 020 | AP | 1978/01/09 | Control Supplement | | 008943 | 019 | AP | 1977/06/29 | Control Supplement | | 008943 | 018 | AP | 1977/06/29 | Formulation Revision | | 008943 | 017 | AP | 1977/06/06 | Expiration Date Change | | 008943 | 015 | AP | 1977/01/28 | Expiration Date Change | | 008943 | 013 | AP | 1977/01/28 | Formulation Revision | | 008943 | 000 | AP | 1953/07/27 | Approval |
|