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
71335-1851-7	71335-1851	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20241211	N/A	ANDA	ANDA203270	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-7)
71335-1851-8	71335-1851	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20241211	N/A	ANDA	ANDA203270	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-8)
72162-2388-5	72162-2388	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240828	N/A	ANDA	ANDA203270	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2388-5)
72162-2388-6	72162-2388	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240828	N/A	ANDA	ANDA203270	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2388-6)
72162-2388-9	72162-2388	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20240828	N/A	ANDA	ANDA203270	Bryant Ranch Prepack	OMEPRAZOLE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2388-9)
57237-160-01	57237-160	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20150819	N/A	ANDA	ANDA203270	Rising Pharma Holdings, Inc.	OMEPRAZOLE	10 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-160-01)
57237-160-30	57237-160	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20150819	N/A	ANDA	ANDA203270	Rising Pharma Holdings, Inc.	OMEPRAZOLE	10 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-160-30)
50090-7366-0	50090-7366	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20241018	N/A	ANDA	ANDA203270	A-S Medication Solutions	OMEPRAZOLE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7366-0)
50090-7366-1	50090-7366	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20241018	N/A	ANDA	ANDA203270	A-S Medication Solutions	OMEPRAZOLE	40 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7366-1)
50090-7366-2	50090-7366	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 (50090-7366-2)
50090-7366-3	50090-7366	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20241018	N/A	ANDA	ANDA203270	A-S Medication Solutions	OMEPRAZOLE	40 mg/1	28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7366-3)
57237-161-50	57237-161	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20150819	N/A	ANDA	ANDA203270	Rising Pharma Holdings, Inc.	OMEPRAZOLE	20 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-50)
57237-161-90	57237-161	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20150819	N/A	ANDA	ANDA203270	Rising Pharma Holdings, Inc.	OMEPRAZOLE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-90)
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)
57237-161-99	57237-161	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20150819	N/A	ANDA	ANDA203270	Rising Pharma Holdings, Inc.	OMEPRAZOLE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-99)
51655-452-25	51655-452	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230202	N/A	ANDA	ANDA203270	Northwind Health Company, LLC	OMEPRAZOLE	40 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-452-25)
51655-452-26	51655-452	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20220926	N/A	ANDA	ANDA203270	Northwind Health Company, LLC	OMEPRAZOLE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-452-26)