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1. 列表页商品名字段中有红色标记P代表该数据有专利信息；当使用各个专利到期时间检索条件时，“有无专利”默认为有。


2. 批准日期显示1982-01-01的，实际为1982-01-01之前。


3. 更多参比制剂一次性进口信息

你目前无法使用部分二次筛选功能 请联系客服开通更多权限和功能！
导出数据
申请号 产品号 商品名 活性成分 活性成分 剂型/给药途径 规格/剂量 申请机构 批准时间 参比制剂 标准制剂 市场状态 TE
(ANDA) 074832 001 CAPTOPRIL AND HYDROCHLOROTHIAZIDE CAPTOPRIL; HYDROCHLOROTHIAZIDE 卡托普利;氢氯噻嗪 TABLET;ORAL 50MG;25MG WATSON LABS 1997-12-29 No No DISCN
(ANDA) 214442 002 CAPTOPRIL CAPTOPRIL 卡托普利 TABLET;ORAL 25MG AIPING PHARM INC 2023-01-27 No No RX AB
(ANDA) 214442 003 CAPTOPRIL CAPTOPRIL 卡托普利 TABLET;ORAL 50MG AIPING PHARM INC 2023-01-27 No No RX AB
(ANDA) 214442 004 CAPTOPRIL CAPTOPRIL 卡托普利 TABLET;ORAL 100MG AIPING PHARM INC 2023-01-27 No No RX AB
(ANDA) 212809 001 CAPTOPRIL CAPTOPRIL 卡托普利 TABLET;ORAL 12.5MG AJANTA PHARMA LTD 2019-12-13 No No RX AB
(ANDA) 212809 002 CAPTOPRIL CAPTOPRIL 卡托普利 TABLET;ORAL 25MG AJANTA PHARMA LTD 2019-12-13 No No RX AB
(ANDA) 212809 003 CAPTOPRIL CAPTOPRIL 卡托普利 TABLET;ORAL 50MG AJANTA PHARMA LTD 2019-12-13 No No RX AB
(ANDA) 212809 004 CAPTOPRIL CAPTOPRIL 卡托普利 TABLET;ORAL 100MG AJANTA PHARMA LTD 2019-12-13 No No RX AB
(ANDA) 074677 004 CAPTOPRIL CAPTOPRIL 卡托普利 TABLET;ORAL 12.5MG ANDAS 5 HOLDING 1997-05-30 No No RX AB
(ANDA) 214442 001 CAPTOPRIL CAPTOPRIL 卡托普利 TABLET;ORAL 12.5MG AIPING PHARM INC 2023-01-27 No No RX AB
(NDA) 018709 003 CAPOZIDE 50/25 CAPTOPRIL; HYDROCHLOROTHIAZIDE 卡托普利;氢氯噻嗪 TABLET;ORAL 50MG;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** APOTHECON 1984-10-12 Yes No DISCN
(NDA) 018709 004 CAPOZIDE 50/15 CAPTOPRIL; HYDROCHLOROTHIAZIDE 卡托普利;氢氯噻嗪 TABLET;ORAL 50MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** APOTHECON 1984-10-12 Yes No DISCN
(NDA) 018343 002 CAPOTEN CAPTOPRIL 卡托普利 TABLET;ORAL 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** STRIDES PHARMA 1982-01-01 Yes No DISCN
(NDA) 018343 006 CAPOTEN CAPTOPRIL 卡托普利 TABLET;ORAL 37.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** STRIDES PHARMA 1986-09-17 Yes No DISCN
(NDA) 018343 001 CAPOTEN CAPTOPRIL 卡托普利 TABLET;ORAL 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** STRIDES PHARMA 1982-01-01 Yes No DISCN
(NDA) 018343 007 CAPOTEN CAPTOPRIL 卡托普利 TABLET;ORAL 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** STRIDES PHARMA 1995-06-13 Yes No DISCN
(NDA) 018343 003 CAPOTEN CAPTOPRIL 卡托普利 TABLET;ORAL 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** STRIDES PHARMA 1982-01-01 Yes No DISCN
(NDA) 018343 004 CAPOTEN CAPTOPRIL 卡托普利 TABLET;ORAL 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** STRIDES PHARMA 1995-06-13 Yes No DISCN
(NDA) 018709 001 CAPOZIDE 25/15 CAPTOPRIL; HYDROCHLOROTHIAZIDE 卡托普利;氢氯噻嗪 TABLET;ORAL 25MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** APOTHECON 1984-10-12 Yes No DISCN
(NDA) 018709 002 CAPOZIDE 25/25 CAPTOPRIL; HYDROCHLOROTHIAZIDE 卡托普利;氢氯噻嗪 TABLET;ORAL 25MG;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** APOTHECON 1984-10-12 Yes No DISCN