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
68788-7742-6	68788-7742	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20200701	N/A	ANDA	ANDA205868	Preferred Pharmaceuticals, Inc.	LANSOPRAZOLE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-6)
68788-7742-8	68788-7742	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20200701	N/A	ANDA	ANDA205868	Preferred Pharmaceuticals, Inc.	LANSOPRAZOLE	30 mg/1	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-8)
68788-7742-9	68788-7742	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20200701	N/A	ANDA	ANDA205868	Preferred Pharmaceuticals, Inc.	LANSOPRAZOLE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-9)
50090-6079-0	50090-6079	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20220919	N/A	ANDA	ANDA205868	A-S Medication Solutions	LANSOPRAZOLE	15 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6079-0)
70756-806-30	70756-806	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20180604	N/A	ANDA	ANDA205868	Lifestar Pharma LLC.	LANSOPRAZOLE	15 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70756-806-30)