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药智数据企业版注册数据库：增设了"联合申报"、"临床试验默认许可日期"等搜索条件，让搜索页面纬度更加全面，还有热点搜索和高级条件组合检索等检索功能 等你来体验！
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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
(NDA) 019593 002 ZANTAC IN PLASTIC CONTAINER RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 INJECTABLE;INJECTION EQ 1MG BASE/ML PAI HOLDINGS PHARM 1991-09-27 No No DISCN
(NDA) 019593 001 ZANTAC IN PLASTIC CONTAINER RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 INJECTABLE;INJECTION EQ 50MG BASE/100ML PAI HOLDINGS PHARM 1986-12-17 No No DISCN
(NDA) 020520 001 ZANTAC 75 RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 TABLET;ORAL EQ 75MG BASE CHATTEM SANOFI 1995-12-19 Yes No DISCN
(NDA) 020745 001 ZANTAC 75 RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 TABLET, EFFERVESCENT;ORAL EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** CHATTEM SANOFI 1998-02-26 Yes No DISCN
(NDA) 018703 002 ZANTAC 300 RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 TABLET;ORAL EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** GLAXO GRP LTD 1985-12-09 Yes No DISCN
(NDA) 020095 002 ZANTAC 300 RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 CAPSULE;ORAL EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** GLAXOSMITHKLINE 1994-03-08 Yes No DISCN
(NDA) 020251 003 ZANTAC 25 RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 TABLET, EFFERVESCENT;ORAL EQ 25MG BASE GLAXO GRP LTD 2004-04-01 No No DISCN
(NDA) 020095 001 ZANTAC 150 RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 CAPSULE;ORAL EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** GLAXOSMITHKLINE 1994-03-08 Yes No DISCN
(NDA) 020251 002 ZANTAC 150 RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 GRANULE, EFFERVESCENT;ORAL EQ 150MG BASE/PACKET GLAXO GRP LTD 1994-03-31 No No DISCN
(NDA) 021698 002 ZANTAC 150 RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 TABLET;ORAL EQ 150MG BASE CHATTEM SANOFI 2007-03-13 Yes No DISCN
(NDA) 020251 001 ZANTAC 150 RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 TABLET, EFFERVESCENT;ORAL EQ 150MG BASE GLAXO GRP LTD 1994-03-31 No No DISCN
(NDA) 021698 001 ZANTAC 150 RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 TABLET;ORAL EQ 150MG BASE CHATTEM SANOFI 2004-08-31 Yes No DISCN
(NDA) 018703 001 ZANTAC 150 RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 TABLET;ORAL EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** GLAXO GRP LTD 1983-06-09 Yes No DISCN
(NDA) 019675 001 ZANTAC RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 SYRUP;ORAL EQ 15MG BASE/ML GLAXO GRP LTD 1988-12-30 Yes No DISCN
(NDA) 019090 001 ZANTAC RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 INJECTABLE;INJECTION EQ 25MG BASE/ML PAI HOLDINGS PHARM 1984-10-19 Yes No DISCN
(ANDA) 075557 001 RANITIDINE HYDROCHLORIDE RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 CAPSULE;ORAL EQ 150MG BASE TEVA 2003-10-31 No No DISCN
(ANDA) 074655 002 RANITIDINE HYDROCHLORIDE RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 CAPSULE;ORAL EQ 300MG BASE SANDOZ 1997-10-22 No Yes RX AB
(ANDA) 074655 001 RANITIDINE HYDROCHLORIDE RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 CAPSULE;ORAL EQ 150MG BASE SANDOZ 1997-10-22 No No RX AB
(ANDA) 075742 001 RANITIDINE HYDROCHLORIDE RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 CAPSULE;ORAL EQ 150MG BASE DR REDDYS LABS LTD 2000-11-29 No No RX AB
(ANDA) 211058 002 RANITIDINE HYDROCHLORIDE RANITIDINE HYDROCHLORIDE 盐酸雷尼替丁 CAPSULE;ORAL EQ 300MG BASE AUROBINDO PHARMA 2018-07-16 No No DISCN