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
67877-274-30	67877-274	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20190120	N/A	ANDA	ANDA207394	Ascend Laboratories, LLC	LANSOPRAZOLE	15 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-274-30)
67877-274-90	67877-274	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20190120	N/A	ANDA	ANDA207394	Ascend Laboratories, LLC	LANSOPRAZOLE	15 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-274-90)
67877-275-05	67877-275	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20210601	N/A	ANDA	ANDA207394	Ascend Laboratories, LLC	LANSOPRAZOLE	30 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-275-05)
67877-275-30	67877-275	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20190120	N/A	ANDA	ANDA207394	Ascend Laboratories, LLC	LANSOPRAZOLE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-275-30)
67877-275-90	67877-275	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20190120	N/A	ANDA	ANDA207394	Ascend Laboratories, LLC	LANSOPRAZOLE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-275-90)
76420-621-90	76420-621	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20231005	N/A	ANDA	ANDA207394	Asclemed USA, Inc.	LANSOPRAZOLE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-621-90)
50090-5180-0	50090-5180	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20200928	N/A	ANDA	ANDA207394	A-S Medication Solutions	LANSOPRAZOLE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-5180-0)
50090-5180-1	50090-5180	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20200928	N/A	ANDA	ANDA207394	A-S Medication Solutions	LANSOPRAZOLE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-5180-1)