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
62175-136-43	62175-136	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20090123	N/A	ANDA	ANDA075410	Lannett Company, Inc.	OMEPRAZOLE	40 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-43)
68071-4025-3	68071-4025	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20170731	N/A	ANDA	ANDA075410	NuCare Pharmaceuticals,Inc.	OMEPRAZOLE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-4025-3)
43353-829-60	43353-829	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20130325	N/A	ANDA	ANDA075410	Aphena Pharma Solutions - Tennessee, LLC	OMEPRAZOLE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43353-829-60)
43353-829-80	43353-829	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20201111	N/A	ANDA	ANDA075410	Aphena Pharma Solutions - Tennessee, LLC	OMEPRAZOLE	40 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43353-829-80)
71205-157-60	71205-157	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20181101	N/A	ANDA	ANDA075410	Proficient Rx LP	OMEPRAZOLE	40 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-60)
71205-157-90	71205-157	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20181101	N/A	ANDA	ANDA075410	Proficient Rx LP	OMEPRAZOLE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-90)
71205-157-30	71205-157	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20181101	N/A	ANDA	ANDA075410	Proficient Rx LP	OMEPRAZOLE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-30)