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 |
2021/10/20 |
SUPPL-49(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2020/07/29 |
SUPPL-48(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2020/05/12 |
SUPPL-47(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2019/05/21 |
SUPPL-45(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2019/01/16 |
SUPPL-44(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/07/14 |
SUPPL-40(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2014/05/20 |
SUPPL-39(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2014/01/22 |
SUPPL-37(补充) |
Approval |
Efficacy |
STANDARD
|
|
|
2013/06/28 |
SUPPL-38(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2013/06/28 |
SUPPL-34(补充) |
Approval |
Efficacy |
STANDARD
|
|
|
2013/04/22 |
SUPPL-35(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2013/02/25 |
SUPPL-36(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2012/07/09 |
SUPPL-30(补充) |
Approval |
Labeling |
UNKNOWN
|
|
|
2012/01/03 |
SUPPL-29(补充) |
Approval |
Labeling |
UNKNOWN
|
|
|
2011/07/18 |
SUPPL-28(补充) |
Approval |
Labeling |
UNKNOWN
|
|
|
2010/09/14 |
SUPPL-27(补充) |
Approval |
Labeling |
UNKNOWN
|
|
|
2009/10/02 |
SUPPL-22(补充) |
Approval |
Efficacy |
PRIORITY
|
|
|
2008/05/30 |
SUPPL-21(补充) |
Approval |
Manufacturing (CMC) |
N/A
|
|
|
2008/01/18 |
SUPPL-17(补充) |
Approval |
Efficacy |
UNKNOWN
|
|
|
2007/08/27 |
SUPPL-19(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2006/09/06 |
SUPPL-14(补充) |
Approval |
Efficacy |
STANDARD
|
|
|
2006/07/10 |
SUPPL-15(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2003/11/17 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2003/10/10 |
SUPPL-9(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2003/08/21 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2003/02/11 |
SUPPL-4(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/10/17 |
SUPPL-5(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2002/08/08 |
SUPPL-6(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2002/05/10 |
SUPPL-3(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2001/05/03 |
SUPPL-2(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2001/01/16 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2000/05/26 |
ORIG-1(原始申请) |
Approval |
Type 1 - New Molecular Entity |
STANDARD
|
|
|
与本品相关的专利信息(来自FDA橙皮书Orange Book)
与本品治疗等效的药品
活性成分:COLESEVELAM HYDROCHLORIDE 剂型/给药途径:TABLET;ORAL 规格:625MG 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 |
021176 |
001 |
NDA |
WELCHOL |
COLESEVELAM HYDROCHLORIDE |
TABLET;ORAL |
625MG |
Prescription |
Yes |
Yes |
AB |
2000/05/26
|
COSETTE |
091600 |
001 |
ANDA |
COLESEVELAM HYDROCHLORIDE |
COLESEVELAM HYDROCHLORIDE |
TABLET;ORAL |
625MG |
Prescription |
No |
No |
AB |
2018/05/16
|
IMPAX LABS INC |
203480 |
001 |
ANDA |
COLESEVELAM HYDROCHLORIDE |
COLESEVELAM HYDROCHLORIDE |
TABLET;ORAL |
625MG |
Prescription |
No |
No |
AB |
2018/05/18
|
GLENMARK PHARMS LTD |
209038 |
001 |
ANDA |
COLESEVELAM HYDROCHLORIDE |
COLESEVELAM HYDROCHLORIDE |
TABLET;ORAL |
625MG |
Prescription |
No |
No |
AB |
2018/10/05
|
ALKEM LABS LTD |
210889 |
001 |
ANDA |
COLESEVELAM HYDROCHLORIDE |
COLESEVELAM HYDROCHLORIDE |
TABLET;ORAL |
625MG |
Prescription |
No |
No |
AB |
2018/10/05
|
DR REDDYS |
208670 |
001 |
ANDA |
COLESEVELAM HYDROCHLORIDE |
COLESEVELAM HYDROCHLORIDE |
TABLET;ORAL |
625MG |
Prescription |
No |
No |
AB |
2019/09/13
|
BIONPHARMA |
207765 |
001 |
ANDA |
COLESEVELAM HYDROCHLORIDE |
COLESEVELAM HYDROCHLORIDE |
TABLET;ORAL |
625MG |
Prescription |
No |
No |
AB |
2019/10/07
|
ZYDUS PHARMS |
209946 |
001 |
ANDA |
COLESEVELAM HYDROCHLORIDE |
COLESEVELAM HYDROCHLORIDE |
TABLET;ORAL |
625MG |
Prescription |
No |
No |
AB |
2020/07/15
|
ZHEJIANG JINGXIN |
212050 |
001 |
ANDA |
COLESEVELAM HYDROCHLORIDE |
COLESEVELAM HYDROCHLORIDE |
TABLET;ORAL |
625MG |
Prescription |
No |
No |
AB |
2020/12/04
|
INVENTIA |
206036 |
001 |
ANDA |
COLESEVELAM HYDROCHLORIDE |
COLESEVELAM HYDROCHLORIDE |
TABLET;ORAL |
625MG |
Prescription |
No |
No |
AB |
2021/10/14
|
BEIJING TIDE PHARM |
213456 |
001 |
ANDA |
COLESEVELAM HYDROCHLORIDE |
COLESEVELAM HYDROCHLORIDE |
TABLET;ORAL |
625MG |
Discontinued |
No |
No |
AB |
2022/01/21
|
UNITED RES LABS |