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
68001-112-04	68001-112	HUMAN PRESCRIPTION DRUG	Lansoprazole	lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20200831	N/A	ANDA	ANDA091269	BluePoint Laboratories	LANSOPRAZOLE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-04)
68001-112-05	68001-112	HUMAN PRESCRIPTION DRUG	Lansoprazole	lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20131201	N/A	ANDA	ANDA091269	BluePoint Laboratories	LANSOPRAZOLE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-05)
63187-510-30	63187-510	HUMAN PRESCRIPTION DRUG	Lansoprazole	lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20150701	N/A	ANDA	ANDA091269	Proficient Rx LP	LANSOPRAZOLE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-510-30)
63187-510-60	63187-510	HUMAN PRESCRIPTION DRUG	Lansoprazole	lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20150701	N/A	ANDA	ANDA091269	Proficient Rx LP	LANSOPRAZOLE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-510-60)
63187-510-90	63187-510	HUMAN PRESCRIPTION DRUG	Lansoprazole	lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20150701	N/A	ANDA	ANDA091269	Proficient Rx LP	LANSOPRAZOLE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-510-90)