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-54(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2021/03/04 |
SUPPL-53(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2019/10/07 |
SUPPL-52(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/09/21 |
SUPPL-51(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/09/18 |
SUPPL-50(补充) |
Approval |
REMS |
|
|
|
2017/08/29 |
SUPPL-49(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2017/08/29 |
SUPPL-48(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/12/16 |
SUPPL-47(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/12/16 |
SUPPL-46(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/03/20 |
SUPPL-45(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2013/05/14 |
SUPPL-44(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2011/06/23 |
SUPPL-43(补充) |
Approval |
Labeling |
|
|
|
2008/06/05 |
SUPPL-42(补充) |
Approval |
Labeling |
|
|
|
2007/10/18 |
SUPPL-41(补充) |
Approval |
Labeling |
|
|
|
2002/09/03 |
SUPPL-35(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2002/09/03 |
SUPPL-34(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2002/09/03 |
SUPPL-32(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2002/09/03 |
SUPPL-31(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2000/01/28 |
SUPPL-30(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1995/01/09 |
SUPPL-28(补充) |
Approval |
Labeling |
|
|
|
1995/01/09 |
SUPPL-27(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1995/01/09 |
SUPPL-26(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1995/01/05 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1989/06/29 |
SUPPL-25(补充) |
Approval |
Labeling |
|
|
|
1988/08/25 |
SUPPL-24(补充) |
Approval |
Labeling |
|
|
|
1987/02/06 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/02/06 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/02/06 |
SUPPL-17(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/02/06 |
SUPPL-16(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1986/02/21 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1980/01/23 |
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:ACETAMINOPHEN; CODEINE PHOSPHATE 剂型/给药途径:TABLET;ORAL 规格:300MG;60MG 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 |
087083 |
001 |
ANDA |
ACETAMINOPHEN AND CODEINE PHOSPHATE |
ACETAMINOPHEN; CODEINE PHOSPHATE |
TABLET;ORAL |
300MG;60MG |
Prescription |
No |
No |
AA |
Approved Prior to Jan 1, 1982
|
SUN PHARM INDS LTD |
088629 |
001 |
ANDA |
ACETAMINOPHEN AND CODEINE PHOSPHATE |
ACETAMINOPHEN; CODEINE PHOSPHATE |
TABLET;ORAL |
300MG;60MG |
Discontinued |
Yes |
No |
AA |
1985/03/06
|
NOSTRUM LABS INC |
089828 |
001 |
ANDA |
ACETAMINOPHEN AND CODEINE PHOSPHATE |
ACETAMINOPHEN; CODEINE PHOSPHATE |
TABLET;ORAL |
300MG;60MG |
Prescription |
No |
No |
AA |
1988/09/30
|
STRIDES PHARMA |
040419 |
003 |
ANDA |
ACETAMINOPHEN AND CODEINE PHOSPHATE |
ACETAMINOPHEN; CODEINE PHOSPHATE |
TABLET;ORAL |
300MG;60MG |
Prescription |
No |
Yes |
AA |
2001/05/31
|
SPECGX LLC |
202800 |
003 |
ANDA |
ACETAMINOPHEN AND CODEINE PHOSPHATE |
ACETAMINOPHEN; CODEINE PHOSPHATE |
TABLET;ORAL |
300MG;60MG |
Prescription |
No |
No |
AA |
2013/04/15
|
AUROLIFE PHARMA LLC |
211610 |
003 |
ANDA |
ACETAMINOPHEN AND CODEINE PHOSPHATE |
ACETAMINOPHEN; CODEINE PHOSPHATE |
TABLET;ORAL |
300MG;60MG |
Prescription |
No |
No |
AA |
2019/06/27
|
WES PHARMA INC |
212418 |
003 |
ANDA |
ACETAMINOPHEN AND CODEINE PHOSPHATE |
ACETAMINOPHEN; CODEINE PHOSPHATE |
TABLET;ORAL |
300MG;60MG |
Prescription |
No |
No |
AA |
2019/09/10
|
ELITE LABS INC |