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 |
2020/06/18 |
SUPPL-46(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/09/10 |
SUPPL-45(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2017/11/28 |
SUPPL-44(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2017/04/10 |
SUPPL-43(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2017/02/24 |
SUPPL-42(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/12/23 |
SUPPL-41(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2012/05/31 |
SUPPL-40(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2011/11/18 |
SUPPL-39(补充) |
Approval |
Labeling |
901 REQUIRED
|
|
|
2010/05/17 |
SUPPL-36(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2009/11/06 |
SUPPL-35(补充) |
Approval |
Efficacy |
PRIORITY
|
|
|
2008/09/19 |
SUPPL-33(补充) |
Approval |
Efficacy |
PRIORITY
|
|
|
2006/11/15 |
SUPPL-32(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2006/05/10 |
SUPPL-29(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2003/10/15 |
SUPPL-27(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/12/18 |
SUPPL-26(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/02/21 |
SUPPL-25(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2001/10/05 |
SUPPL-24(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2001/03/30 |
SUPPL-21(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2000/02/01 |
SUPPL-23(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/02/26 |
SUPPL-22(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/03/04 |
SUPPL-19(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1998/02/25 |
SUPPL-20(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1996/10/04 |
SUPPL-18(补充) |
Approval |
Efficacy |
STANDARD
|
|
|
1996/10/04 |
SUPPL-15(补充) |
Approval |
Efficacy |
UNKNOWN
|
|
|
1995/07/20 |
SUPPL-16(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1995/02/06 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1994/10/07 |
SUPPL-12(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1994/08/08 |
SUPPL-11(补充) |
Approval |
Efficacy |
PRIORITY
|
|
|
1994/08/08 |
SUPPL-7(补充) |
Approval |
Labeling |
|
|
|
1993/08/24 |
SUPPL-10(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1992/10/19 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1990/05/25 |
SUPPL-1(补充) |
Approval |
Labeling |
|
|
|
1990/05/02 |
SUPPL-2(补充) |
Approval |
Efficacy |
|
|
|
1990/03/02 |
SUPPL-4(补充) |
Approval |
Efficacy |
|
|
|
1990/01/12 |
SUPPL-3(补充) |
Approval |
Efficacy |
|
|
|
1989/09/28 |
ORIG-1(原始申请) |
Approval |
Type 3 - New Dosage Form |
PRIORITY
|
|
|
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:ZIDOVUDINE 剂型/给药途径:SOLUTION;ORAL 规格:50MG/5ML 治疗等效代码:AA
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 |
019910 |
001 |
NDA |
RETROVIR |
ZIDOVUDINE |
SOLUTION;ORAL |
50MG/5ML |
Prescription |
Yes |
Yes |
AA |
1989/09/28
|
VIIV HLTHCARE |
077268 |
001 |
ANDA |
ZIDOVUDINE |
ZIDOVUDINE |
SOLUTION;ORAL |
50MG/5ML |
Prescription |
No |
No |
AA |
2005/09/19
|
AUROBINDO |
077981 |
001 |
ANDA |
ZIDOVUDINE |
ZIDOVUDINE |
SOLUTION;ORAL |
50MG/5ML |
Prescription |
No |
No |
AA |
2008/06/26
|
CIPLA LTD |