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)
62175-136-46	62175-136	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20090123	N/A	ANDA	ANDA075410	Lannett Company, Inc.	OMEPRAZOLE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-46)
62175-114-46	62175-114	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20030903	N/A	ANDA	ANDA075410	Lannett Company, Inc.	OMEPRAZOLE	10 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-114-46)
68071-4906-9	68071-4906	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20190523	N/A	ANDA	ANDA075410	NuCare Pharmaceuticals,Inc.	OMEPRAZOLE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-4906-9)
62175-114-49	62175-114	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20030903	N/A	ANDA	ANDA075410	Lannett Company, Inc.	OMEPRAZOLE	10 mg/1	72000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-114-49)
62175-114-32	62175-114	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20030903	N/A	ANDA	ANDA075410	Lannett Company, Inc.	OMEPRAZOLE	10 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-114-32)
62175-136-49	62175-136	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20090123	N/A	ANDA	ANDA075410	Lannett Company, Inc.	OMEPRAZOLE	40 mg/1	36000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-136-49)