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
68071-5119-3	68071-5119	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20191220	N/A	ANDA	ANDA205868	NuCare Pharmaceuticals,Inc.	LANSOPRAZOLE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-5119-3)
68071-5119-4	68071-5119	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20191220	N/A	ANDA	ANDA205868	NuCare Pharmaceuticals,Inc.	LANSOPRAZOLE	30 mg/1	14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-5119-4)
71335-1425-5	71335-1425	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20220502	N/A	ANDA	ANDA205868	Bryant Ranch Prepack	LANSOPRAZOLE	30 mg/1	56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-5)
71335-1425-4	71335-1425	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20220502	N/A	ANDA	ANDA205868	Bryant Ranch Prepack	LANSOPRAZOLE	30 mg/1	28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-4)
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)