美国FDA药品数据库-药物在线

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RANITIDINE HYDROCHLORIDE	TABLET;ORAL	EQ 150MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1983/06/09	1983/06/09	GLAXO GRP LTD	Discontinued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RANITIDINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 150MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1994/03/08	1994/03/08	GLAXOSMITHKLINE	Discontinued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	No	2004/08/31	2004/08/31	CHATTEM SANOFI	Discontinued
ZANTAC 150	021698	002	NDA	RANITIDINE HYDROCHLORIDE	TABLET;ORAL	EQ 150MG BASE	Yes	No	2004/08/31	2007/03/13	CHATTEM SANOFI	Discontinued