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
57237-162-01	57237-162	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20150819	N/A	ANDA	ANDA203270	Rising Pharma Holdings, Inc.	OMEPRAZOLE	40 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-01)
50090-7367-0	50090-7367	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20241018	N/A	ANDA	ANDA203270	A-S Medication Solutions	OMEPRAZOLE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7367-0)
57237-162-10	57237-162	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20150819	N/A	ANDA	ANDA203270	Rising Pharma Holdings, Inc.	OMEPRAZOLE	40 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-10)
57237-162-30	57237-162	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20150819	N/A	ANDA	ANDA203270	Rising Pharma Holdings, Inc.	OMEPRAZOLE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-30)
57237-162-50	57237-162	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20150819	N/A	ANDA	ANDA203270	Rising Pharma Holdings, Inc.	OMEPRAZOLE	40 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-50)
57237-162-90	57237-162	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20150819	N/A	ANDA	ANDA203270	Rising Pharma Holdings, Inc.	OMEPRAZOLE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-90)