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 |
2014/02/21 |
SUPPL-30(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/02/21 |
SUPPL-19(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/02/21 |
SUPPL-18(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/02/21 |
SUPPL-17(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/02/21 |
SUPPL-16(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2014/02/21 |
SUPPL-14(补充) |
Approval |
Labeling |
|
|
|
2002/12/18 |
SUPPL-24(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2002/09/05 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2002/04/29 |
SUPPL-23(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2001/10/11 |
SUPPL-22(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2001/03/16 |
SUPPL-21(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
1995/01/06 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
1986/01/27 |
SUPPL-12(补充) |
Approval |
Labeling |
|
|
|
1986/01/27 |
SUPPL-8(补充) |
Approval |
Labeling |
|
|
|
1986/01/27 |
SUPPL-7(补充) |
Approval |
Labeling |
|
|
|
1986/01/08 |
SUPPL-13(补充) |
Approval |
Labeling |
|
|
|
1985/07/30 |
SUPPL-11(补充) |
Approval |
Labeling |
|
|
|
1985/03/08 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
1983/11/28 |
SUPPL-9(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
1981/09/14 |
SUPPL-5(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
1980/07/21 |
SUPPL-4(补充) |
Approval |
Labeling |
|
|
|
1980/03/28 |
SUPPL-3(补充) |
Approval |
Labeling |
|
|
|
1977/09/28 |
SUPPL-1(补充) |
Approval |
Labeling |
|
|
|
1977/04/25 |
ORIG-1(原始申请) |
Approval |
Type 3 - New Dosage Form |
PRIORITY
|
|
|
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:CARBIDOPA 剂型/给药途径:TABLET;ORAL 规格:25MG 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 |
017830 |
001 |
NDA |
LODOSYN |
CARBIDOPA |
TABLET;ORAL |
25MG |
Prescription |
Yes |
Yes |
AB |
Approved Prior to Jan 1, 1982
|
ATON |
203261 |
001 |
ANDA |
CARBIDOPA |
CARBIDOPA |
TABLET;ORAL |
25MG |
Discontinued |
No |
No |
AB |
2014/03/10
|
ANI PHARMS |
204291 |
001 |
ANDA |
CARBIDOPA |
CARBIDOPA |
TABLET;ORAL |
25MG |
Prescription |
No |
No |
AB |
2016/01/08
|
ALVOGEN |
205304 |
001 |
ANDA |
CARBIDOPA |
CARBIDOPA |
TABLET;ORAL |
25MG |
Prescription |
No |
No |
AB |
2016/02/17
|
EDENBRIDGE PHARMS |
204763 |
001 |
ANDA |
CARBIDOPA |
CARBIDOPA |
TABLET;ORAL |
25MG |
Prescription |
No |
No |
AB |
2017/10/20
|
NOVEL LABS INC |
209910 |
001 |
ANDA |
CARBIDOPA |
CARBIDOPA |
TABLET;ORAL |
25MG |
Prescription |
No |
No |
AB |
2018/05/07
|
ZYDUS PHARMS |
211055 |
001 |
ANDA |
CARBIDOPA |
CARBIDOPA |
TABLET;ORAL |
25MG |
Prescription |
No |
No |
AB |
2019/10/21
|
AUROBINDO PHARMA |
217961 |
001 |
ANDA |
CARBIDOPA |
CARBIDOPA |
TABLET;ORAL |
25MG |
Prescription |
No |
No |
AB |
2023/12/11
|
BEXIMCO PHARMS USA |