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 |
2022/11/09 |
SUPPL-72(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2022/11/09 |
SUPPL-63(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/07/18 |
SUPPL-55(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/07/11 |
SUPPL-54(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/07/01 |
SUPPL-53(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2009/07/08 |
SUPPL-43(补充) |
Approval |
Labeling |
|
|
|
2008/08/13 |
SUPPL-40(补充) |
Approval |
Labeling |
|
|
|
2007/06/25 |
SUPPL-37(补充) |
Approval |
Labeling |
|
|
|
2005/11/29 |
SUPPL-27(补充) |
Approval |
Labeling |
|
|
|
2005/07/08 |
SUPPL-26(补充) |
Approval |
Labeling |
|
|
|
2002/11/12 |
SUPPL-23(补充) |
Approval |
Labeling |
|
|
|
2001/03/30 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2000/10/25 |
SUPPL-17(补充) |
Approval |
Labeling |
|
|
|
2000/07/07 |
SUPPL-16(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/03/22 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/03/22 |
SUPPL-14(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1996/10/04 |
SUPPL-12(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1996/04/22 |
SUPPL-11(补充) |
Approval |
Labeling |
|
|
|
1995/04/21 |
SUPPL-10(补充) |
Approval |
Labeling |
|
|
|
1994/05/11 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1994/01/11 |
SUPPL-9(补充) |
Approval |
Labeling |
|
|
|
1993/05/18 |
SUPPL-7(补充) |
Approval |
Labeling |
|
|
|
1992/04/30 |
SUPPL-6(补充) |
Approval |
Labeling |
|
|
|
1991/12/16 |
SUPPL-5(补充) |
Approval |
Labeling |
|
|
|
1988/09/20 |
SUPPL-3(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1988/05/26 |
SUPPL-2(补充) |
Approval |
Labeling |
|
|
|
1988/05/26 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1988/03/09 |
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:TRAZODONE 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 |
071525 |
001 |
ANDA |
TRAZODONE HYDROCHLORIDE |
TRAZODONE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
1988/03/09
|
PLIVA |
073137 |
003 |
ANDA |
TRAZODONE HYDROCHLORIDE |
TRAZODONE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
1995/12/22
|
SUN PHARM INDUSTRIES |
071196 |
002 |
ANDA |
TRAZODONE HYDROCHLORIDE |
TRAZODONE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
1999/04/26
|
APOTEX INC |
202180 |
003 |
ANDA |
TRAZODONE HYDROCHLORIDE |
TRAZODONE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2013/11/27
|
TORRENT |
206923 |
003 |
ANDA |
TRAZODONE HYDROCHLORIDE |
TRAZODONE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2017/09/08
|
ACCORD HLTHCARE |
205253 |
003 |
ANDA |
TRAZODONE HYDROCHLORIDE |
TRAZODONE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2017/10/10
|
ZYDUS PHARMS |
204852 |
003 |
ANDA |
TRAZODONE HYDROCHLORIDE |
TRAZODONE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2020/02/05
|
AUROBINDO PHARMA |
211116 |
003 |
ANDA |
TRAZODONE HYDROCHLORIDE |
TRAZODONE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2024/05/20
|
CROSSMEDIKA SA |
218988 |
003 |
ANDA |
TRAZODONE HYDROCHLORIDE |
TRAZODONE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2024/08/08
|
GRANULES |
217740 |
003 |
ANDA |
TRAZODONE HYDROCHLORIDE |
TRAZODONE HYDROCHLORIDE |
TABLET;ORAL |
150MG |
Prescription |
No |
No |
AB |
2024/08/27
|
GRAVITI PHARMS |