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 |
2023/12/15 |
SUPPL-45(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2021/09/13 |
SUPPL-43(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2021/06/02 |
SUPPL-41(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2019/10/07 |
SUPPL-38(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/02/01 |
SUPPL-32(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/12/16 |
SUPPL-29(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/09/22 |
SUPPL-27(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2014/06/02 |
SUPPL-26(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2008/02/04 |
SUPPL-21(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2005/08/03 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2005/08/03 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2005/05/26 |
SUPPL-16(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2005/05/26 |
SUPPL-15(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/03/27 |
SUPPL-14(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2000/04/03 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1993/04/20 |
SUPPL-12(补充) |
Approval |
Labeling |
|
|
|
1982/09/07 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1981/11/25 |
SUPPL-9(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1980/02/06 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1980/02/06 |
SUPPL-7(补充) |
Approval |
Labeling |
|
|
|
1977/02/11 |
SUPPL-2(补充) |
Approval |
Labeling |
|
|
|
1976/08/06 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1973/03/14 |
ORIG-1(原始申请) |
Approval |
Type 3 - New Dosage Form |
STANDARD
|
|
|
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:CONCENTRATE;ORAL 规格:10MG/ML 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 |
017116 |
002 |
NDA |
METHADOSE |
METHADONE HYDROCHLORIDE |
CONCENTRATE;ORAL |
10MG/ML |
Prescription |
Yes |
Yes |
AA |
Approved Prior to Jan 1, 1982
|
SPECGX LLC |
089897 |
001 |
ANDA |
METHADONE HYDROCHLORIDE INTENSOL |
METHADONE HYDROCHLORIDE |
CONCENTRATE;ORAL |
10MG/ML |
Prescription |
No |
No |
AA |
1988/09/06
|
HIKMA |
040088 |
001 |
ANDA |
METHADONE HYDROCHLORIDE |
METHADONE HYDROCHLORIDE |
CONCENTRATE;ORAL |
10MG/ML |
Prescription |
No |
No |
AA |
1994/11/30
|
VISTAPHARM LLC |
040180 |
001 |
ANDA |
METHADONE HYDROCHLORIDE |
METHADONE HYDROCHLORIDE |
CONCENTRATE;ORAL |
10MG/ML |
Prescription |
No |
No |
AA |
1998/04/30
|
HIKMA |
207368 |
001 |
ANDA |
METHADONE HYDROCHLORIDE |
METHADONE HYDROCHLORIDE |
CONCENTRATE;ORAL |
10MG/ML |
Prescription |
No |
No |
AA |
2019/08/22
|
SPECGX LLC |
212093 |
001 |
ANDA |
METHADONE HYDROCHLORIDE |
METHADONE HYDROCHLORIDE |
CONCENTRATE;ORAL |
10MG/ML |
Prescription |
No |
No |
AA |
2020/11/02
|
LANNETT CO INC |