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
>>>原始批准或临时批准<<<
| 审批日期 | 提交号 | 审批结论 | 提交分类 | 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 |
| 1985/04/18 |
ORIG-1(原始申请) |
Approval |
|
|
|
|
>>>补充申请<<<
| 审批日期 | 提交号 | 审批结论 | 补充类别或审批类型 | 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 |
| 2004/08/04 |
SUPPL-32(补充) |
Approval |
Labeling |
|
|
|
| 2000/01/19 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC)-Manufacturing Process |
|
|
|
| 1999/06/25 |
SUPPL-30(补充) |
Approval |
Labeling |
|
|
|
| 1999/03/22 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1998/08/25 |
SUPPL-27(补充) |
Approval |
Labeling |
|
|
|
| 1998/07/30 |
SUPPL-26(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1998/02/25 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1998/02/05 |
SUPPL-24(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1996/05/20 |
SUPPL-23(补充) |
Approval |
Labeling |
|
|
|
| 1993/10/29 |
SUPPL-22(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1993/03/19 |
SUPPL-20(补充) |
Approval |
Labeling |
|
|
|
| 1992/07/16 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1992/07/16 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1992/07/16 |
SUPPL-17(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1992/07/16 |
SUPPL-16(补充) |
Approval |
Labeling |
|
|
|
| 1992/07/16 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1990/12/17 |
SUPPL-14(补充) |
Approval |
Labeling |
|
|
|
| 1990/01/31 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1989/05/05 |
SUPPL-11(补充) |
Approval |
Labeling |
|
|
|
| 1988/07/01 |
SUPPL-9(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1988/07/01 |
SUPPL-5(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1986/07/09 |
SUPPL-4(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1986/04/17 |
SUPPL-2(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1986/01/22 |
SUPPL-3(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
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 |
| 无 |
与本品治疗等效的药品
>>>活性成分:METHYLDOPA; 剂型/给药途径:TABLET;ORAL; 规格:250MG; 治疗等效代码:AB<<<
| 申请号 | 产品号 | 申请类型 | 商品名 | 活性成分 | 剂型/给药途径 | 规格 | 市场状态 | RLD | RS | TE Code | 产品号批准日期 | 申请人 |
| 070075 |
001 |
ANDA |
METHYLDOPA |
METHYLDOPA |
TABLET;ORAL |
250MG |
Prescription |
No |
No |
AB |
--
|
MYLAN |