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
ZEGERID	021636	001	NDA	OMEPRAZOLE; SODIUM BICARBONATE	FOR SUSPENSION;ORAL	20MG/PACKET;1.68GM/PACKET	Yes	No	2004/06/15	2004/06/15	SALIX	Discontinued
ZEGERID	021636	002	NDA	OMEPRAZOLE; SODIUM BICARBONATE	FOR SUSPENSION;ORAL	40MG/PACKET;1.68GM/PACKET	Yes	No	2004/06/15	2004/12/21	SALIX	Discontinued
ZEGERID	021706	001	NDA	OMEPRAZOLE; SODIUM BICARBONATE	FOR SUSPENSION; ORAL	40MG/PACKET;1.68GM/PACKET	Yes	No	2004/12/21	--	SANTARUS	Discontinued
ZEGERID	021849	001	NDA	OMEPRAZOLE; SODIUM BICARBONATE	CAPSULE;ORAL	20MG;1.1GM	Yes	No	2006/02/27	2006/02/27	SALIX	Discontinued
ZEGERID	021849	002	NDA	OMEPRAZOLE; SODIUM BICARBONATE	CAPSULE;ORAL	40MG;1.1GM	Yes	No	2006/02/27	2006/02/27	SALIX	Discontinued
ZEGERID	021850	001	NDA	MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE	TABLET, CHEWABLE;ORAL	700MG;20MG;600MG	No	No	2006/03/24	2006/03/24	SANTARUS	Discontinued
ZEGERID	021850	002	NDA	MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE	TABLET, CHEWABLE;ORAL	700MG;40MG;600MG	No	No	2006/03/24	2006/03/24	SANTARUS	Discontinued
ZEGERID OTC	022281	001	NDA	OMEPRAZOLE; SODIUM BICARBONATE	CAPSULE;ORAL	20MG;1.1GM	Yes	Yes	2009/12/01	2009/12/01	RILEY CONSUMER	Over-the-counter
ZEGERID OTC	022283	001	NDA	OMEPRAZOLE; SODIUM BICARBONATE	FOR SUSPENSION;ORAL	20MG/PACKET;1.68GM/PACKET	Yes	Yes	2013/06/17	2013/06/17	RILEY CONSUMER	Over-the-counter