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 |
2016/04/19 |
SUPPL-57(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2013/05/08 |
SUPPL-56(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2010/10/19 |
SUPPL-54(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2007/01/24 |
SUPPL-53(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2003/03/26 |
SUPPL-46(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/08/01 |
SUPPL-51(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2002/06/03 |
SUPPL-50(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2001/07/02 |
SUPPL-49(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2000/12/06 |
SUPPL-48(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1998/04/16 |
SUPPL-47(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1997/04/07 |
SUPPL-45(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1988/06/20 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1986/09/16 |
SUPPL-6(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1985/09/16 |
SUPPL-5(补充) |
Approval |
Labeling |
|
|
|
1984/10/24 |
SUPPL-4(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1984/04/24 |
SUPPL-3(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1983/02/17 |
SUPPL-2(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1983/01/26 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/12/21 |
SUPPL-44(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/12/21 |
SUPPL-43(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/06/28 |
SUPPL-42(补充) |
Approval |
Labeling |
|
|
|
1982/02/05 |
SUPPL-41(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1981/07/06 |
SUPPL-37(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1981/03/05 |
SUPPL-34(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1981/03/02 |
SUPPL-33(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1980/11/21 |
SUPPL-31(补充) |
Approval |
Labeling |
|
|
|
1980/11/21 |
SUPPL-24(补充) |
Approval |
Labeling |
|
|
|
1980/08/13 |
SUPPL-32(补充) |
Approval |
Labeling |
|
|
|
1980/01/21 |
SUPPL-27(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1980/01/04 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1980/01/04 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1979/04/10 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1978/01/17 |
SUPPL-22(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1977/07/26 |
SUPPL-21(补充) |
Approval |
Labeling |
|
|
|
1977/04/20 |
SUPPL-20(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1976/12/08 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1976/11/18 |
SUPPL-18(补充) |
Approval |
Labeling |
|
|
|
1976/11/18 |
SUPPL-17(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1976/10/01 |
SUPPL-16(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1976/09/16 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1976/08/04 |
SUPPL-15(补充) |
Approval |
Labeling |
|
|
|
1976/04/01 |
SUPPL-12(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1976/01/16 |
SUPPL-11(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1975/07/16 |
SUPPL-9(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1975/06/20 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1975/04/16 |
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:GRISEOFULVIN, ULTRAMICROSIZE 剂型/给药途径:TABLET;ORAL 规格:125MG 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 |
050475 |
001 |
NDA |
GRIS-PEG |
GRISEOFULVIN, ULTRAMICROSIZE |
TABLET;ORAL |
125MG |
Prescription |
Yes |
No |
AB |
Approved Prior to Jan 1, 1982
|
BAUSCH |
061996 |
001 |
ANDA |
FULVICIN P/G |
GRISEOFULVIN, ULTRAMICROSIZE |
TABLET;ORAL |
125MG |
Prescription |
No |
No |
AB |
Approved Prior to Jan 1, 1982
|
CHARTWELL RX |
202545 |
001 |
ANDA |
GRISEOFULVIN,ULTRAMICROSIZE |
GRISEOFULVIN, ULTRAMICROSIZE |
TABLET;ORAL |
125MG |
Prescription |
No |
No |
AB |
2012/10/22
|
SIGMAPHARM LABS LLC |
204371 |
001 |
ANDA |
GRISEOFULVIN, ULTRAMICROSIZE |
GRISEOFULVIN, ULTRAMICROSIZE |
TABLET;ORAL |
125MG |
Prescription |
No |
No |
AB |
2014/01/09
|
MOUNTAIN |
202805 |
001 |
ANDA |
GRISEOFULVIN, ULTRAMICROSIZE |
GRISEOFULVIN, ULTRAMICROSIZE |
TABLET;ORAL |
125MG |
Prescription |
No |
No |
AB |
2018/12/26
|
SANDOZ |
活性成分:GRISEOFULVIN, ULTRAMICROSIZE 剂型/给药途径:TABLET;ORAL 规格:250MG 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 |
050475 |
002 |
NDA |
GRIS-PEG |
GRISEOFULVIN, ULTRAMICROSIZE |
TABLET;ORAL |
250MG |
Prescription |
Yes |
No |
AB |
Approved Prior to Jan 1, 1982
|
BAUSCH |
061996 |
002 |
ANDA |
FULVICIN P/G |
GRISEOFULVIN, ULTRAMICROSIZE |
TABLET;ORAL |
250MG |
Prescription |
No |
No |
AB |
Approved Prior to Jan 1, 1982
|
CHARTWELL RX |
202545 |
002 |
ANDA |
GRISEOFULVIN,ULTRAMICROSIZE |
GRISEOFULVIN, ULTRAMICROSIZE |
TABLET;ORAL |
250MG |
Prescription |
No |
No |
AB |
2012/10/22
|
SIGMAPHARM LABS LLC |
204371 |
002 |
ANDA |
GRISEOFULVIN, ULTRAMICROSIZE |
GRISEOFULVIN, ULTRAMICROSIZE |
TABLET;ORAL |
250MG |
Prescription |
No |
Yes |
AB |
2014/01/09
|
MOUNTAIN |
202805 |
002 |
ANDA |
GRISEOFULVIN, ULTRAMICROSIZE |
GRISEOFULVIN, ULTRAMICROSIZE |
TABLET;ORAL |
250MG |
Prescription |
No |
No |
AB |
2018/12/26
|
SANDOZ |