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
31722-571-05	31722-571	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20200518	N/A	ANDA	ANDA203083	Camber Pharmaceuticals, Inc.	LANSOPRAZOLE	30 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-05)
31722-571-10	31722-571	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20200518	N/A	ANDA	ANDA203083	Camber Pharmaceuticals, Inc.	LANSOPRAZOLE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-10)
31722-571-30	31722-571	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20200518	N/A	ANDA	ANDA203083	Camber Pharmaceuticals, Inc.	LANSOPRAZOLE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-30)
31722-571-90	31722-571	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20200518	N/A	ANDA	ANDA203083	Camber Pharmaceuticals, Inc.	LANSOPRAZOLE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-90)
68071-3634-3	68071-3634	HUMAN PRESCRIPTION DRUG	Lansoprazole	Lansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20240625	N/A	ANDA	ANDA203083	NuCare Pharmaceuticals,Inc.	LANSOPRAZOLE	15 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3634-3)