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
72162-1907-3	72162-1907	HUMAN PRESCRIPTION DRUG	Omeprazole and Sodium Bicarbonate	omeprazole, sodium bicarbonate	POWDER, FOR SUSPENSION	ORAL	20240321	N/A	NDA AUTHORIZED GENERIC	NDA021636	Bryant Ranch Prepack	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1680 mg/1	30 PACKET in 1 CARTON (72162-1907-3) / 1 POWDER, FOR SUSPENSION in 1 PACKET
68682-990-30	68682-990	HUMAN PRESCRIPTION DRUG	Omeprazole and Sodium Bicarbonate	omeprazole, sodium bicarbonate	POWDER, FOR SUSPENSION	ORAL	20040615	N/A	NDA AUTHORIZED GENERIC	NDA021636	Oceanside Pharmaceuticals	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1680 mg/1	30 PACKET in 1 CARTON (68682-990-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET
68682-991-30	68682-991	HUMAN PRESCRIPTION DRUG	Omeprazole and Sodium Bicarbonate	omeprazole, sodium bicarbonate	POWDER, FOR SUSPENSION	ORAL	20040615	N/A	NDA AUTHORIZED GENERIC	NDA021636	Oceanside Pharmaceuticals	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1680 mg/1	30 PACKET in 1 CARTON (68682-991-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET
72162-1906-3	72162-1906	HUMAN PRESCRIPTION DRUG	Omeprazole and Sodium Bicarbonate	omeprazole, sodium bicarbonate	POWDER, FOR SUSPENSION	ORAL	20240321	N/A	NDA AUTHORIZED GENERIC	NDA021636	Bryant Ranch Prepack	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1680 mg/1	30 PACKET in 1 CARTON (72162-1906-3) / 1 POWDER, FOR SUSPENSION in 1 PACKET
68012-054-03	68012-054	HUMAN PRESCRIPTION DRUG	ZEGERID	omeprazole and sodium bicarbonate	POWDER, FOR SUSPENSION	ORAL	20140615	N/A	NDA	NDA021636	Santarus, Inc..	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1680 mg/1	3 PACKET in 1 CARTON (68012-054-03) / 1 POWDER, FOR SUSPENSION in 1 PACKET
68012-054-30	68012-054	HUMAN PRESCRIPTION DRUG	ZEGERID	omeprazole and sodium bicarbonate	POWDER, FOR SUSPENSION	ORAL	20140615	N/A	NDA	NDA021636	Santarus, Inc..	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1680 mg/1	30 PACKET in 1 CARTON (68012-054-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET
68012-052-30	68012-052	HUMAN PRESCRIPTION DRUG	ZEGERID	omeprazole and sodium bicarbonate	POWDER, FOR SUSPENSION	ORAL	20040615	N/A	NDA	NDA021636	Santarus, Inc..	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1680 mg/1	30 PACKET in 1 CARTON (68012-052-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET