美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ZEGERID"
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 Prescription
ZEGERID 021636 002 NDA OMEPRAZOLE; SODIUM BICARBONATE FOR SUSPENSION;ORAL 40MG/PACKET;1.68GM/PACKET Yes Yes 2004/06/15 2004/12/21 SALIX Prescription
ZEGERID 021706 001 NDA OMEPRAZOLE; SODIUM BICARBONATE FOR SUSPENSION; ORAL 40MG/PACKET;1.68GM/PACKET Yes 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 SANTARUS INC Prescription
ZEGERID 021849 002 NDA OMEPRAZOLE; SODIUM BICARBONATE CAPSULE;ORAL 40MG;1.1GM Yes Yes 2006/02/27 2006/02/27 SANTARUS INC Prescription
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 BAYER HEALTHCARE LLC 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 BAYER HEALTHCARE LLC Over-the-counter
药品名称,活性成分,申请号搜索 高级检索
©2006-2019 DrugFuture->U.S. FDA Drugs Database