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 |
2024/10/31 |
SUPPL-45(补充) |
Approval |
REMS |
|
|
|
2023/12/15 |
SUPPL-43(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2021/06/02 |
SUPPL-41(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2019/10/09 |
SUPPL-40(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/09/21 |
SUPPL-39(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/09/18 |
SUPPL-38(补充) |
Approval |
REMS |
|
|
|
2018/02/01 |
SUPPL-37(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/01/31 |
SUPPL-36(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2017/05/26 |
SUPPL-35(补充) |
Approval |
REMS |
|
|
|
2017/03/10 |
SUPPL-33(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/12/16 |
SUPPL-31(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/12/16 |
SUPPL-30(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/12/15 |
SUPPL-28(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/09/30 |
SUPPL-32(补充) |
Approval |
REMS |
|
|
|
2016/04/20 |
SUPPL-29(补充) |
Approval |
REMS |
|
|
|
2015/06/26 |
SUPPL-27(补充) |
Approval |
REMS |
|
|
|
2014/08/19 |
SUPPL-26(补充) |
Approval |
REMS |
|
|
|
2014/04/16 |
SUPPL-24(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2013/04/15 |
SUPPL-23(补充) |
Approval |
REMS |
|
|
|
2012/07/09 |
SUPPL-22(补充) |
Approval |
REMS |
|
|
|
2012/07/09 |
SUPPL-21(补充) |
Approval |
Labeling |
|
|
|
2008/01/02 |
SUPPL-19(补充) |
Approval |
Labeling |
|
|
|
2007/06/07 |
SUPPL-18(补充) |
Approval |
Labeling |
|
|
|
2000/02/01 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/03/03 |
SUPPL-14(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/03/03 |
SUPPL-12(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/03/02 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/03/02 |
SUPPL-11(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/03/02 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1996/08/28 |
SUPPL-9(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1994/01/31 |
SUPPL-4(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1991/12/24 |
SUPPL-8(补充) |
Approval |
Labeling |
|
|
|
1991/12/24 |
SUPPL-5(补充) |
Approval |
Labeling |
|
|
|
1988/02/04 |
SUPPL-3(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1982/08/30 |
ORIG-1(原始申请) |
Approval |
|
|
|
|
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:METHADONE HYDROCHLORIDE 剂型/给药途径:SOLUTION;ORAL 规格:10MG/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 |
087997 |
001 |
ANDA |
METHADONE HYDROCHLORIDE |
METHADONE HYDROCHLORIDE |
SOLUTION;ORAL |
10MG/5ML |
Prescription |
Yes |
Yes |
AA |
1982/08/30
|
HIKMA |
090707 |
002 |
ANDA |
METHADONE HYDROCHLORIDE |
METHADONE HYDROCHLORIDE |
SOLUTION;ORAL |
10MG/5ML |
Discontinued |
No |
No |
AA |
2010/06/30
|
VISTAPHARM LLC |
207537 |
002 |
ANDA |
METHADONE HYDROCHLORIDE |
METHADONE HYDROCHLORIDE |
SOLUTION;ORAL |
10MG/5ML |
Prescription |
No |
No |
AA |
2019/10/01
|
SPECGX LLC |