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 |
2022/10/13 |
SUPPL-69(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2020/02/05 |
SUPPL-67(补充) |
Approval |
Labeling |
901 REQUIRED
|
|
|
2018/12/20 |
SUPPL-65(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/04/30 |
SUPPL-64(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/05/27 |
SUPPL-59(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2015/05/11 |
SUPPL-58(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2015/01/05 |
SUPPL-57(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2011/10/20 |
SUPPL-56(补充) |
Approval |
Labeling |
901 REQUIRED
|
|
|
2006/10/01 |
SUPPL-55(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2006/04/07 |
SUPPL-51(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/10/07 |
SUPPL-49(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/10/07 |
SUPPL-46(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/10/07 |
SUPPL-40(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/10/07 |
SUPPL-35(补充) |
Approval |
Labeling |
|
|
|
2002/10/07 |
SUPPL-27(补充) |
Approval |
Labeling |
|
|
|
2002/10/07 |
SUPPL-25(补充) |
Approval |
Labeling |
|
|
|
2001/10/16 |
SUPPL-48(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2000/12/22 |
SUPPL-47(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1997/07/11 |
SUPPL-45(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1995/05/26 |
SUPPL-43(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1990/05/02 |
SUPPL-37(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1990/04/20 |
SUPPL-34(补充) |
Approval |
Labeling |
|
|
|
1989/04/07 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1988/10/13 |
SUPPL-32(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1988/10/13 |
SUPPL-31(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1988/08/24 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1986/05/01 |
SUPPL-24(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1985/05/29 |
SUPPL-21(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1985/03/26 |
SUPPL-22(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1984/03/26 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1983/02/25 |
SUPPL-20(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1983/02/25 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/04/19 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/02/19 |
SUPPL-17(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1981/09/25 |
SUPPL-16(补充) |
Approval |
Labeling |
|
|
|
1981/08/06 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1981/04/06 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1980/10/02 |
SUPPL-10(补充) |
Approval |
Labeling |
|
|
|
1980/05/13 |
SUPPL-9(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1980/01/04 |
SUPPL-3(补充) |
Approval |
Labeling |
|
|
|
1979/10/03 |
SUPPL-5(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1979/10/03 |
SUPPL-4(补充) |
Approval |
Labeling |
|
|
|
1979/10/03 |
SUPPL-2(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1979/09/13 |
SUPPL-1(补充) |
Approval |
Labeling |
|
|
|
1979/04/27 |
ORIG-1(原始申请) |
Approval |
Type 5 - New Formulation or New Manufacturer |
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:LITHIUM CARBONATE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:300MG 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 |
018027 |
001 |
NDA |
LITHOBID |
LITHIUM CARBONATE |
TABLET, EXTENDED RELEASE;ORAL |
300MG |
Prescription |
Yes |
Yes |
AB |
Approved Prior to Jan 1, 1982
|
ANI PHARMS |
076832 |
001 |
ANDA |
LITHIUM CARBONATE |
LITHIUM CARBONATE |
TABLET, EXTENDED RELEASE;ORAL |
300MG |
Prescription |
No |
No |
AB |
2004/10/28
|
HIKMA |
091544 |
001 |
ANDA |
LITHIUM CARBONATE |
LITHIUM CARBONATE |
TABLET, EXTENDED RELEASE;ORAL |
300MG |
Prescription |
No |
No |
AB |
2010/12/27
|
GLENMARK PHARMS INC |
202288 |
001 |
ANDA |
LITHIUM CARBONATE |
LITHIUM CARBONATE |
TABLET, EXTENDED RELEASE;ORAL |
300MG |
Prescription |
No |
No |
AB |
2012/06/29
|
MYLAN PHARMS INC |
204779 |
001 |
ANDA |
LITHIUM CARBONATE |
LITHIUM CARBONATE |
TABLET, EXTENDED RELEASE;ORAL |
300MG |
Prescription |
No |
No |
AB |
2015/07/27
|
UNIQUE |
205532 |
001 |
ANDA |
LITHIUM CARBONATE |
LITHIUM CARBONATE |
TABLET, EXTENDED RELEASE;ORAL |
300MG |
Prescription |
No |
No |
AB |
2016/09/29
|
HERITAGE PHARMA |