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
70756-807-51	70756-807	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20180604	N/A	ANDA	ANDA205868	Lifestar Pharma LLC.	LANSOPRAZOLE	30 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70756-807-51)
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)
70756-807-90	70756-807	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20180604	N/A	ANDA	ANDA205868	Lifestar Pharma LLC.	LANSOPRAZOLE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70756-807-90)
80425-0174-1	80425-0174	HUMAN PRESCRIPTION DRUG	Lansoprazole DR	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20180604	N/A	ANDA	ANDA205868	Advanced Rx Pharmacy of Tennessee, LLC	LANSOPRAZOLE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0174-1)
72189-370-30	72189-370	HUMAN PRESCRIPTION DRUG	Lansoprazole DR	Lansoprazole DR	CAPSULE, DELAYED RELEASE	ORAL	20220808	N/A	ANDA	ANDA205868	Direct_Rx	LANSOPRAZOLE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-370-30)