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
27241-029-31	27241-029	HUMAN PRESCRIPTION DRUG	Omeprazole and Sodium Bicarbonate	Omeprazole and Sodium Bicarbonate	FOR SUSPENSION	ORAL	20160727	N/A	ANDA	ANDA205545	Ajanta Pharma USA Inc.	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1680 mg/1	30 FOR SUSPENSION in 1 CARTON (27241-029-31)
27241-029-62	27241-029	HUMAN PRESCRIPTION DRUG	Omeprazole and Sodium Bicarbonate	Omeprazole and Sodium Bicarbonate	FOR SUSPENSION	ORAL	20160727	N/A	ANDA	ANDA205545	Ajanta Pharma USA Inc.	OMEPRAZOLE; SODIUM BICARBONATE	20 mg/1; 1680 mg/1	1 FOR SUSPENSION in 1 PACKET (27241-029-62)
27241-030-31	27241-030	HUMAN PRESCRIPTION DRUG	Omeprazole and Sodium Bicarbonate	Omeprazole and Sodium Bicarbonate	FOR SUSPENSION	ORAL	20160727	N/A	ANDA	ANDA205545	Ajanta Pharma USA Inc.	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1680 mg/1	30 FOR SUSPENSION in 1 CARTON (27241-030-31)
27241-030-62	27241-030	HUMAN PRESCRIPTION DRUG	Omeprazole and Sodium Bicarbonate	Omeprazole and Sodium Bicarbonate	FOR SUSPENSION	ORAL	20160727	N/A	ANDA	ANDA205545	Ajanta Pharma USA Inc.	OMEPRAZOLE; SODIUM BICARBONATE	40 mg/1; 1680 mg/1	1 FOR SUSPENSION in 1 PACKET (27241-030-62)