药品注册申请号:017808
申请类型:NDA (新药申请)
申请人:MYLAN IRELAND LTD
申请人全名:MYLAN IRELAND LTD
产品信息
产品号商品名活性成分剂型/给药途径规格/剂量参比药物(RLD)生物等效参考标准(RS)治疗等效代码该申请号批准日期该产品号批准日期市场状态
001 MIACALCIN CALCITONIN SALMON INJECTABLE;INJECTION 100 IU/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None 1986/07/03 1986/07/03 Discontinued
002 MIACALCIN CALCITONIN SALMON INJECTABLE;INJECTION 200 IU/ML Yes Yes AP 1991/03/29 Prescription
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
2017/09/11 SUPPL-37(补充) Approval Labeling STANDARD
2015/02/02 SUPPL-36(补充) Approval Labeling STANDARD
2014/03/11 SUPPL-35(补充) Approval Labeling STANDARD
2013/02/19 SUPPL-33(补充) Approval Manufacturing (CMC) STANDARD
2012/04/18 SUPPL-34(补充) Approval Labeling STANDARD
2009/10/30 SUPPL-30(补充) Approval Labeling STANDARD
2003/06/03 SUPPL-24(补充) Approval Labeling STANDARD
2002/02/12 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
2001/11/02 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1999/07/23 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1999/05/26 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1999/01/13 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1998/12/24 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1997/08/01 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1997/07/14 SUPPL-14(补充) Approval Labeling STANDARD
1997/01/02 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1996/08/14 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1995/06/09 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1994/07/22 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1993/03/26 SUPPL-3(补充) Approval Labeling
1993/02/22 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1992/08/05 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1992/06/26 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1992/06/10 SUPPL-6(补充) Approval Labeling
1992/06/01 SUPPL-7(补充) Approval Labeling
1991/10/03 SUPPL-2(补充) Approval Labeling
1991/03/29 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1986/07/03 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
与本品相关的市场独占权保护信息
关联产品号独占权代码失效日期备注
与本品治疗等效的药品
活性成分:CALCITONIN SALMON 剂型/给药途径:INJECTABLE;INJECTION 规格:200 IU/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RLDRSTE Code产品号批准日期申请人
215715 001 ANDA CALCITONIN-SALMON CALCITONIN SALMON INJECTABLE;INJECTION 200 IU/ML Prescription No No AP -- DR REDDYS
017808 002 NDA MIACALCIN CALCITONIN SALMON INJECTABLE;INJECTION 200 IU/ML Prescription Yes Yes AP 1991/03/29 MYLAN IRELAND LTD
212416 001 ANDA CALCITONIN-SALMON CALCITONIN SALMON INJECTABLE;INJECTION 200 IU/ML Prescription No No AP 2021/05/14 CUSTOPHARM INC
209358 001 ANDA CALCITONIN-SALMON CALCITONIN SALMON INJECTABLE;INJECTION 200 IU/ML Prescription No No AP 2021/11/10 PAR STERILE PRODUCTS
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