美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ZANTAC 150"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
ZANTAC 150 018703 001 NDA RANITIDINE HYDROCHLORIDE TABLET;ORAL EQ 150MG BASE Yes No 1983/06/09 1983/06/09 GLAXO GRP LTD Discontinued
ZANTAC 150 020095 001 NDA RANITIDINE HYDROCHLORIDE CAPSULE;ORAL EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1994/03/08 1994/03/08 GLAXOSMITHKLINE Discontinued
ZANTAC 150 020251 001 NDA RANITIDINE HYDROCHLORIDE TABLET, EFFERVESCENT;ORAL EQ 150MG BASE No No 1994/03/31 1994/03/31 GLAXO GRP LTD Discontinued
ZANTAC 150 020251 002 NDA RANITIDINE HYDROCHLORIDE GRANULE, EFFERVESCENT;ORAL EQ 150MG BASE/PACKET No No 1994/03/31 1994/03/31 GLAXO GRP LTD Discontinued
ZANTAC 150 021698 001 NDA RANITIDINE HYDROCHLORIDE TABLET;ORAL EQ 150MG BASE Yes Yes 2004/08/31 2004/08/31 SANOFI US Over-the-counter
ZANTAC 150 021698 002 NDA RANITIDINE HYDROCHLORIDE TABLET;ORAL EQ 150MG BASE Yes No 2004/08/31 2007/03/13 SANOFI US Over-the-counter
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