美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
68012-102-30	68012-102	HUMAN PRESCRIPTION DRUG	ZEGERID	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20060227	N/A	NDA	NDA021849	Santarus, Inc..	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1100 mg/1	30 CAPSULE in 1 BOTTLE (68012-102-30)
68012-104-05	68012-104	HUMAN PRESCRIPTION DRUG	ZEGERID	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20060227	N/A	NDA	NDA021849	Santarus, Inc..	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1100 mg/1	5 CAPSULE in 1 BOTTLE (68012-104-05)
68012-104-30	68012-104	HUMAN PRESCRIPTION DRUG	ZEGERID	omeprazole and sodium bicarbonate	CAPSULE	ORAL	20060227	N/A	NDA	NDA021849	Santarus, Inc..	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1100 mg/1	30 CAPSULE in 1 BOTTLE (68012-104-30)
68682-104-30	68682-104	HUMAN PRESCRIPTION DRUG	Omeprazole and Sodium Bicarbonate	omeprazole, sodium bicarbonate	CAPSULE	ORAL	20070227	N/A	NDA AUTHORIZED GENERIC	NDA021849	Oceanside Pharmaceuticals	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1100 mg/1	30 CAPSULE in 1 BOTTLE (68682-104-30)
68682-102-30	68682-102	HUMAN PRESCRIPTION DRUG	Omeprazole and Sodium Bicarbonate	omeprazole, sodium bicarbonate	CAPSULE	ORAL	20060227	N/A	NDA AUTHORIZED GENERIC	NDA021849	Oceanside Pharmaceuticals	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1100 mg/1	30 CAPSULE in 1 BOTTLE (68682-102-30)