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 |
2009/09/04 |
SUPPL-53(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2009/02/17 |
SUPPL-51(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2006/07/12 |
SUPPL-50(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/03/14 |
SUPPL-47(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2002/01/15 |
SUPPL-46(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2002/01/07 |
SUPPL-45(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2001/11/06 |
SUPPL-41(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2001/05/09 |
SUPPL-44(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1999/10/29 |
SUPPL-43(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1999/10/29 |
SUPPL-37(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1999/10/22 |
SUPPL-40(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1999/10/22 |
SUPPL-39(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1999/04/02 |
SUPPL-42(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1998/01/14 |
SUPPL-38(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1994/11/03 |
SUPPL-35(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1993/04/05 |
SUPPL-32(补充) |
Approval |
Labeling |
|
|
|
1992/07/22 |
SUPPL-31(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1992/05/19 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1991/11/25 |
SUPPL-24(补充) |
Approval |
Labeling |
|
|
|
1991/09/05 |
SUPPL-30(补充) |
Approval |
Labeling |
|
|
|
1990/12/20 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1990/12/12 |
SUPPL-26(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1990/11/21 |
SUPPL-27(补充) |
Approval |
Labeling |
|
|
|
1990/09/26 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1990/08/13 |
SUPPL-17(补充) |
Approval |
Efficacy |
|
|
|
1990/07/16 |
SUPPL-25(补充) |
Approval |
Labeling |
|
|
|
1990/06/25 |
SUPPL-21(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1989/08/08 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1989/05/18 |
SUPPL-20(补充) |
Approval |
Labeling |
|
|
|
1989/03/17 |
SUPPL-16(补充) |
Approval |
Labeling |
|
|
|
1989/03/17 |
SUPPL-13(补充) |
Approval |
Labeling |
|
|
|
1988/05/20 |
SUPPL-15(补充) |
Approval |
Labeling |
|
|
|
1988/05/20 |
SUPPL-14(补充) |
Approval |
Labeling |
|
|
|
1988/05/19 |
SUPPL-12(补充) |
Approval |
Labeling |
|
|
|
1988/03/03 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1987/11/24 |
SUPPL-11(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1987/04/09 |
SUPPL-9(补充) |
Approval |
Labeling |
|
|
|
1987/04/09 |
SUPPL-5(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1987/04/09 |
SUPPL-4(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1986/08/08 |
SUPPL-6(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1986/02/28 |
SUPPL-3(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1985/08/08 |
SUPPL-2(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1985/04/16 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1984/10/19 |
ORIG-1(原始申请) |
Approval |
Type 3 - New Dosage Form |
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:RANITIDINE HYDROCHLORIDE 剂型/给药途径:INJECTABLE;INJECTION 规格:EQ 25MG BASE/ML 治疗等效代码:AP
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 |
019090 |
001 |
NDA |
ZANTAC |
RANITIDINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
EQ 25MG BASE/ML |
Discontinued |
Yes |
No |
AP |
1984/10/19
|
PAI HOLDINGS PHARM |
074777 |
001 |
ANDA |
RANITIDINE HYDROCHLORIDE |
RANITIDINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
EQ 25MG BASE/ML |
Discontinued |
No |
No |
AP |
2005/03/02
|
HIKMA |
077458 |
001 |
ANDA |
RANITIDINE HYDROCHLORIDE |
RANITIDINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
EQ 25MG BASE/ML |
Discontinued |
No |
No |
AP |
2006/02/16
|
HIKMA |
091534 |
001 |
ANDA |
RANITIDINE HYDROCHLORIDE |
RANITIDINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
EQ 25MG BASE/ML |
Discontinued |
No |
No |
AP |
2013/02/22
|
ZYDUS PHARMS USA INC |
079076 |
001 |
ANDA |
RANITIDINE HYDROCHLORIDE |
RANITIDINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
EQ 25MG BASE/ML |
Discontinued |
No |
No |
AP |
2016/06/09
|
MYLAN LABS LTD |