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 |
2016/04/25 |
SUPPL-74(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/07/17 |
SUPPL-72(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2007/11/13 |
SUPPL-65(补充) |
Approval |
Labeling |
|
|
|
2007/06/29 |
SUPPL-64(补充) |
Approval |
Labeling |
|
|
|
2005/06/09 |
SUPPL-62(补充) |
Approval |
Labeling |
|
|
|
2002/12/16 |
SUPPL-61(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2001/06/25 |
SUPPL-60(补充) |
Approval |
Labeling |
|
|
|
2001/03/23 |
SUPPL-59(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2000/08/07 |
SUPPL-58(补充) |
Approval |
Labeling |
|
|
|
1999/05/05 |
SUPPL-57(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/05/28 |
SUPPL-56(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1996/11/18 |
SUPPL-55(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1995/04/10 |
SUPPL-54(补充) |
Approval |
Labeling |
|
|
|
1995/02/01 |
SUPPL-53(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1993/08/27 |
SUPPL-52(补充) |
Approval |
Labeling |
|
|
|
1992/12/15 |
SUPPL-51(补充) |
Approval |
Labeling |
|
|
|
1987/07/17 |
SUPPL-50(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/07/17 |
SUPPL-48(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/07/17 |
SUPPL-45(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/07/17 |
SUPPL-44(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/07/17 |
SUPPL-43(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/07/17 |
SUPPL-42(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/07/17 |
SUPPL-41(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/04/27 |
SUPPL-49(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/01/08 |
SUPPL-47(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/01/08 |
SUPPL-46(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/01/08 |
SUPPL-40(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1985/03/22 |
SUPPL-36(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1985/03/22 |
SUPPL-35(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1984/01/25 |
SUPPL-34(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1983/07/27 |
SUPPL-32(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1983/07/27 |
SUPPL-30(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1983/07/27 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1983/03/21 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1982/06/23 |
SUPPL-27(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1982/06/23 |
SUPPL-24(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1977/11/21 |
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:AMITRIPTYLINE HYDROCHLORIDE 剂型/给药途径:TABLET;ORAL 规格:150MG 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 |
085970 |
001 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
--
|
SANDOZ |
085968 |
005 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
Yes |
No |
AB |
Approved Prior to Jan 1, 1982
|
SANDOZ |
089399 |
006 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
1987/07/14
|
SUN PHARM INDS INC |
040218 |
006 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Discontinued |
No |
No |
AB |
1997/09/11
|
ENDO OPERATIONS |
202446 |
006 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2014/06/04
|
ACCORD HLTHCARE |
210086 |
006 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2017/10/06
|
ZYDUS PHARMS |
213999 |
006 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2021/02/19
|
MANKIND PHARMA |
214548 |
006 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2021/05/19
|
UNICHEM |
212654 |
006 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2021/09/29
|
AIPING PHARM INC |
216243 |
006 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2022/06/06
|
BRECKENRIDGE |
215376 |
006 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2023/05/01
|
RUBICON |
217411 |
006 |
ANDA |
AMITRIPTYLINE HYDROCHLORIDE |
AMITRIPTYLINE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2023/05/19
|
RISING |