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
62135-530-30	62135-530	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230316	N/A	ANDA	ANDA075410	Chartwell RX, LLC	OMEPRAZOLE	10 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62135-530-30)
62135-530-90	62135-530	HUMAN PRESCRIPTION DRUG	Omeprazole	Omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20230316	N/A	ANDA	ANDA075410	Chartwell RX, LLC	OMEPRAZOLE	10 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62135-530-90)
62175-118-32	62175-118	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20021104	N/A	ANDA	ANDA075410	Lannett Company, Inc.	OMEPRAZOLE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-32)
62175-118-37	62175-118	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20021104	N/A	ANDA	ANDA075410	Lannett Company, Inc.	OMEPRAZOLE	20 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-37)
62175-118-43	62175-118	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20021104	N/A	ANDA	ANDA075410	Lannett Company, Inc.	OMEPRAZOLE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-43)
62175-118-46	62175-118	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20021104	N/A	ANDA	ANDA075410	Lannett Company, Inc.	OMEPRAZOLE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-46)
62175-118-49	62175-118	HUMAN PRESCRIPTION DRUG	Omeprazole	omeprazole	CAPSULE, DELAYED RELEASE	ORAL	20021104	N/A	ANDA	ANDA075410	Lannett Company, Inc.	OMEPRAZOLE	20 mg/1	54000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-118-49)