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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！
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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
(NDA) 205410 001 HEMANGEOLP PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 SOLUTION;ORAL 4.28MG/ML PIERRE FABRE 2014-03-14 Yes Yes RX
(NDA) 021438 001 INNOPRAN XL PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 CAPSULE, EXTENDED RELEASE;ORAL 80MG ANI PHARMS 2003-03-12 Yes No RX BX
(NDA) 021438 002 INNOPRAN XL PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 CAPSULE, EXTENDED RELEASE;ORAL 120MG ANI PHARMS 2003-03-12 Yes Yes RX BX
(NDA) 018553 001 INDERAL LA PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 CAPSULE, EXTENDED RELEASE;ORAL 160MG ANI PHARMS 1983-04-19 Yes Yes RX AB
(NDA) 018553 002 INDERAL LA PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 CAPSULE, EXTENDED RELEASE;ORAL 80MG ANI PHARMS 1983-04-19 Yes No RX AB
(NDA) 018553 003 INDERAL LA PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 CAPSULE, EXTENDED RELEASE;ORAL 120MG ANI PHARMS 1983-04-19 Yes No RX AB
(NDA) 018553 004 INDERAL LA PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 CAPSULE, EXTENDED RELEASE;ORAL 60MG ANI PHARMS 1987-03-18 Yes No RX AB
(NDA) 018031 001 INDERIDE-40/25 HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE 氢氯噻嗪;盐酸普萘洛尔 TABLET;ORAL 25MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** WYETH PHARMS INC 1982-01-01 Yes No DISCN
(NDA) 018031 002 INDERIDE-80/25 HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE 氢氯噻嗪;盐酸普萘洛尔 TABLET;ORAL 25MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** WYETH PHARMS INC 1982-01-01 Yes No DISCN
(NDA) 016419 001 PROPRANOLOL HYDROCHLORIDE PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 INJECTABLE;INJECTION 1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** BAXTER HLTHCARE CORP 1982-01-01 Yes No DISCN
(NDA) 016418 001 INDERAL PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 TABLET;ORAL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** WYETH PHARMS 1982-01-01 Yes No DISCN
(NDA) 016418 002 INDERAL PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 TABLET;ORAL 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** WYETH PHARMS 1982-01-01 Yes No DISCN
(NDA) 016418 003 INDERAL PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 TABLET;ORAL 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** WYETH PHARMS 1982-01-01 Yes No DISCN
(NDA) 016418 004 INDERAL PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 TABLET;ORAL 80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** WYETH PHARMS 1982-01-01 Yes No DISCN
(NDA) 016418 009 INDERAL PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 TABLET;ORAL 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** WYETH PHARMS 1982-10-18 Yes No DISCN
(NDA) 016418 010 INDERAL PROPRANOLOL HYDROCHLORIDE 盐酸普萘洛尔 TABLET;ORAL 90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** WYETH PHARMS 1982-10-18 Yes No DISCN