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 |
2021/11/01 |
SUPPL-8(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2019/11/29 |
SUPPL-4(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2019/11/29 |
SUPPL-1(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/11/30 |
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:DEXMETHYLPHENIDATE HYDROCHLORIDE 剂型/给药途径:CAPSULE, EXTENDED RELEASE;ORAL 规格:5MG 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 |
021802 |
001 |
NDA |
FOCALIN XR |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
5MG |
Prescription |
Yes |
No |
AB |
2005/05/26
|
SANDOZ |
078908 |
001 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
5MG |
Prescription |
No |
No |
AB |
2013/11/19
|
TEVA PHARMS USA |
079108 |
001 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
5MG |
Prescription |
No |
No |
AB |
2015/08/05
|
IMPAX LABS INC |
202842 |
001 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
5MG |
Prescription |
No |
No |
AB |
2016/11/30
|
ENDO OPERATIONS |
210279 |
001 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
5MG |
Prescription |
No |
No |
AB |
2018/10/09
|
ADARE PHARMS INC |
213813 |
001 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
5MG |
Prescription |
No |
No |
AB |
2020/09/09
|
GRANULES |
206734 |
001 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
5MG |
Prescription |
No |
No |
AB |
2021/11/05
|
SUN PHARM INDS INC |
078992 |
001 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
5MG |
Prescription |
No |
No |
AB |
2021/11/23
|
INTELLIPHARMACEUTICS |
215523 |
001 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
5MG |
Prescription |
No |
No |
AB |
2021/12/08
|
ASCENT PHARMS INC |
活性成分:DEXMETHYLPHENIDATE HYDROCHLORIDE 剂型/给药途径:CAPSULE, EXTENDED RELEASE;ORAL 规格:10MG 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 |
021802 |
002 |
NDA |
FOCALIN XR |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
Yes |
No |
AB |
2005/05/26
|
SANDOZ |
078908 |
002 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2013/11/19
|
TEVA PHARMS USA |
079108 |
002 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2015/08/05
|
IMPAX LABS INC |
202842 |
002 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2016/11/30
|
ENDO OPERATIONS |
210279 |
002 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2018/10/09
|
ADARE PHARMS INC |
213813 |
002 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2020/09/09
|
GRANULES |
206734 |
002 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2021/11/05
|
SUN PHARM INDS INC |
078992 |
002 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2021/11/23
|
INTELLIPHARMACEUTICS |
215523 |
002 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2021/12/08
|
ASCENT PHARMS INC |
活性成分:DEXMETHYLPHENIDATE HYDROCHLORIDE 剂型/给药途径:CAPSULE, EXTENDED RELEASE;ORAL 规格:15MG 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 |
021802 |
004 |
NDA |
FOCALIN XR |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
15MG |
Prescription |
Yes |
No |
AB |
2006/08/01
|
SANDOZ |
078992 |
003 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
15MG |
Prescription |
No |
No |
AB |
2013/11/18
|
INTELLIPHARMACEUTICS |
079108 |
003 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
15MG |
Prescription |
No |
No |
AB |
2014/05/19
|
IMPAX LABS INC |
078908 |
004 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
15MG |
Prescription |
No |
No |
AB |
2014/05/19
|
TEVA PHARMS USA |
202842 |
003 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
15MG |
Prescription |
No |
No |
AB |
2016/11/30
|
ENDO OPERATIONS |
210279 |
003 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
15MG |
Prescription |
No |
No |
AB |
2018/10/09
|
ADARE PHARMS INC |
213813 |
003 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
15MG |
Prescription |
No |
No |
AB |
2020/09/09
|
GRANULES |
206734 |
003 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
15MG |
Prescription |
No |
No |
AB |
2021/11/05
|
SUN PHARM INDS INC |
215523 |
003 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
15MG |
Prescription |
No |
No |
AB |
2021/12/08
|
ASCENT PHARMS INC |
活性成分:DEXMETHYLPHENIDATE HYDROCHLORIDE 剂型/给药途径:CAPSULE, EXTENDED RELEASE;ORAL 规格:20MG 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 |
021802 |
003 |
NDA |
FOCALIN XR |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
20MG |
Prescription |
Yes |
No |
AB |
2005/05/26
|
SANDOZ |
078908 |
003 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
20MG |
Prescription |
No |
No |
AB |
2013/11/19
|
TEVA PHARMS USA |
079108 |
004 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
20MG |
Prescription |
No |
No |
AB |
2015/12/21
|
IMPAX LABS INC |
202842 |
004 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
20MG |
Prescription |
No |
No |
AB |
2016/11/30
|
ENDO OPERATIONS |
210279 |
004 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
20MG |
Prescription |
No |
No |
AB |
2018/10/09
|
ADARE PHARMS INC |
213813 |
004 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
20MG |
Prescription |
No |
No |
AB |
2020/09/09
|
GRANULES |
206734 |
004 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
20MG |
Prescription |
No |
No |
AB |
2021/11/05
|
SUN PHARM INDS INC |
078992 |
005 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
20MG |
Prescription |
No |
No |
AB |
2021/11/23
|
INTELLIPHARMACEUTICS |
215523 |
004 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
20MG |
Prescription |
No |
No |
AB |
2021/12/08
|
ASCENT PHARMS INC |
活性成分:DEXMETHYLPHENIDATE HYDROCHLORIDE 剂型/给药途径:CAPSULE, EXTENDED RELEASE;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 |
021802 |
008 |
NDA |
FOCALIN XR |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
25MG |
Prescription |
Yes |
No |
AB |
2011/04/21
|
SANDOZ |
202842 |
005 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
25MG |
Prescription |
No |
No |
AB |
2016/11/30
|
ENDO OPERATIONS |
203614 |
001 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
25MG |
Prescription |
No |
No |
AB |
2017/07/05
|
IMPAX LABS INC |
202731 |
001 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
25MG |
Prescription |
No |
No |
AB |
2017/07/05
|
TEVA PHARMS USA |
210279 |
005 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
25MG |
Prescription |
No |
No |
AB |
2018/10/09
|
ADARE PHARMS INC |
213813 |
005 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
25MG |
Prescription |
No |
No |
AB |
2020/09/09
|
GRANULES |
206734 |
005 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
25MG |
Prescription |
No |
No |
AB |
2021/11/05
|
SUN PHARM INDS INC |
215523 |
005 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
25MG |
Prescription |
No |
No |
AB |
2021/12/08
|
ASCENT PHARMS INC |
活性成分:DEXMETHYLPHENIDATE HYDROCHLORIDE 剂型/给药途径:CAPSULE, EXTENDED RELEASE;ORAL 规格:30MG 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 |
021802 |
005 |
NDA |
FOCALIN XR |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
30MG |
Prescription |
Yes |
No |
AB |
2009/10/23
|
SANDOZ |
078992 |
004 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
30MG |
Prescription |
No |
No |
AB |
2013/11/18
|
INTELLIPHARMACEUTICS |
079108 |
005 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
30MG |
Prescription |
No |
No |
AB |
2013/11/21
|
IMPAX LABS INC |
202731 |
003 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
30MG |
Prescription |
No |
No |
AB |
2014/05/19
|
TEVA PHARMS USA |
202842 |
006 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
30MG |
Prescription |
No |
No |
AB |
2016/11/30
|
ENDO OPERATIONS |
210279 |
006 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
30MG |
Prescription |
No |
No |
AB |
2018/10/09
|
ADARE PHARMS INC |
213813 |
006 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
30MG |
Prescription |
No |
No |
AB |
2020/09/09
|
GRANULES |
206734 |
006 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
30MG |
Prescription |
No |
No |
AB |
2021/11/05
|
SUN PHARM INDS INC |
215523 |
006 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
30MG |
Prescription |
No |
No |
AB |
2021/12/08
|
ASCENT PHARMS INC |
活性成分:DEXMETHYLPHENIDATE HYDROCHLORIDE 剂型/给药途径:CAPSULE, EXTENDED RELEASE;ORAL 规格:35MG 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 |
021802 |
007 |
NDA |
FOCALIN XR |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
35MG |
Prescription |
Yes |
No |
AB |
2011/04/21
|
SANDOZ |
202842 |
007 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
35MG |
Prescription |
No |
No |
AB |
2016/11/30
|
ENDO OPERATIONS |
203614 |
002 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
35MG |
Prescription |
No |
No |
AB |
2017/07/05
|
IMPAX LABS INC |
202731 |
004 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
35MG |
Prescription |
No |
No |
AB |
2017/07/05
|
TEVA PHARMS USA |
210279 |
007 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
35MG |
Prescription |
No |
No |
AB |
2018/10/09
|
ADARE PHARMS INC |
213813 |
007 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
35MG |
Prescription |
No |
No |
AB |
2020/09/09
|
GRANULES |
206734 |
007 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
35MG |
Prescription |
No |
No |
AB |
2021/11/05
|
SUN PHARM INDS INC |
215523 |
007 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
35MG |
Prescription |
No |
No |
AB |
2021/12/08
|
ASCENT PHARMS INC |
活性成分:DEXMETHYLPHENIDATE HYDROCHLORIDE 剂型/给药途径:CAPSULE, EXTENDED RELEASE;ORAL 规格:40MG 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 |
021802 |
006 |
NDA |
FOCALIN XR |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
40MG |
Prescription |
Yes |
Yes |
AB |
2010/08/11
|
SANDOZ |
202731 |
002 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
40MG |
Prescription |
No |
No |
AB |
2013/11/19
|
TEVA PHARMS USA |
202842 |
008 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
40MG |
Prescription |
No |
No |
AB |
2016/11/30
|
ENDO OPERATIONS |
210279 |
008 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
40MG |
Prescription |
No |
No |
AB |
2018/10/09
|
ADARE PHARMS INC |
213813 |
008 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
40MG |
Prescription |
No |
No |
AB |
2020/09/09
|
GRANULES |
206734 |
008 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
40MG |
Prescription |
No |
No |
AB |
2021/11/05
|
SUN PHARM INDS INC |
078992 |
006 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
40MG |
Prescription |
No |
No |
AB |
2021/11/23
|
INTELLIPHARMACEUTICS |
215523 |
008 |
ANDA |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
DEXMETHYLPHENIDATE HYDROCHLORIDE |
CAPSULE, EXTENDED RELEASE;ORAL |
40MG |
Prescription |
No |
No |
AB |
2021/12/08
|
ASCENT PHARMS INC |