药品注册申请号:087056
申请类型:ANDA (仿制药申请)
申请人:HERITAGE PHARMA
申请人全名:HERITAGE PHARMA LABS INC
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 CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Yes No AA 1980/01/10 Approved Prior to Jan 1, 1982 Discontinued
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
2009/03/20 SUPPL-45(补充) Approval Labeling
2002/10/04 SUPPL-36(补充) Approval Manufacturing (CMC)
2002/07/29 SUPPL-37(补充) Approval Manufacturing (CMC)
2001/09/12 SUPPL-35(补充) Approval Manufacturing (CMC)
2000/10/26 SUPPL-34(补充) Approval Labeling
2000/07/25 SUPPL-33(补充) Approval Manufacturing (CMC)
2000/01/28 SUPPL-32(补充) Approval Manufacturing (CMC)
1999/09/24 SUPPL-31(补充) Approval Manufacturing (CMC)
1999/09/24 SUPPL-29(补充) Approval Manufacturing (CMC)
1999/09/24 SUPPL-28(补充) Approval Manufacturing (CMC)
1999/08/20 SUPPL-30(补充) Approval Manufacturing (CMC)
1998/12/09 SUPPL-27(补充) Approval Manufacturing (CMC)
1998/03/10 SUPPL-25(补充) Approval Manufacturing (CMC)
1997/10/17 SUPPL-26(补充) Approval Labeling
1997/05/30 SUPPL-24(补充) Approval Manufacturing (CMC)
1994/10/13 SUPPL-22(补充) Approval Manufacturing (CMC)
1989/07/27 SUPPL-21(补充) Approval Labeling
1987/11/12 SUPPL-20(补充) Approval Manufacturing (CMC)
1987/11/12 SUPPL-19(补充) Approval Manufacturing (CMC)
1987/03/06 SUPPL-17(补充) Approval Manufacturing (CMC)
1984/03/08 SUPPL-16(补充) Approval Manufacturing (CMC)
1983/11/02 SUPPL-13(补充) Approval Manufacturing (CMC)
1982/11/12 SUPPL-12(补充) Approval Manufacturing (CMC)
1980/01/10 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
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:CYPROHEPTADINE HYDROCHLORIDE 剂型/给药途径:TABLET;ORAL 规格:4MG 治疗等效代码:AA
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
087056 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Discontinued Yes No AA Approved Prior to Jan 1, 1982 HERITAGE PHARMA
088212 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Prescription No No AA 1983/05/26 CHARTWELL RX
040537 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Prescription No No AA 2003/09/30 MOUNTAIN
040644 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Prescription No No AA 2006/05/30 KENTON
205087 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Prescription No No AA 2015/09/23 NOVAST LABS
206553 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Prescription No No AA 2016/11/29 APPCO
207783 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Discontinued No No AA 2016/12/29 RISING
207555 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Prescription No No AA 2017/01/31 RISING
208938 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Prescription No Yes AA 2017/05/19 ZYDUS PHARMS
209172 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Prescription No No AA 2018/04/11 STRIDES PHARMA
206676 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Prescription No No AA 2019/04/12 BEXIMCO PHARMS USA
212491 001 ANDA CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET;ORAL 4MG Prescription No No AA 2021/02/24 QUAGEN
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