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
69238-1125-1	69238-1125	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170602	N/A	ANDA	ANDA208832	Amneal Pharmaceuticals NY LLC	NADOLOL	80 mg/1	1000 TABLET in 1 BOTTLE (69238-1125-1)
69238-1125-3	69238-1125	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170602	N/A	ANDA	ANDA208832	Amneal Pharmaceuticals NY LLC	NADOLOL	80 mg/1	30 TABLET in 1 BOTTLE (69238-1125-3)
69238-1125-9	69238-1125	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170602	N/A	ANDA	ANDA208832	Amneal Pharmaceuticals NY LLC	NADOLOL	80 mg/1	90 TABLET in 1 BOTTLE (69238-1125-9)
69238-1124-1	69238-1124	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170602	N/A	ANDA	ANDA208832	Amneal Pharmaceuticals NY LLC	NADOLOL	40 mg/1	1000 TABLET in 1 BOTTLE (69238-1124-1)
69238-1124-3	69238-1124	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170602	N/A	ANDA	ANDA208832	Amneal Pharmaceuticals NY LLC	NADOLOL	40 mg/1	30 TABLET in 1 BOTTLE (69238-1124-3)
69238-1124-9	69238-1124	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170602	N/A	ANDA	ANDA208832	Amneal Pharmaceuticals NY LLC	NADOLOL	40 mg/1	90 TABLET in 1 BOTTLE (69238-1124-9)
69238-1123-1	69238-1123	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170602	N/A	ANDA	ANDA208832	Amneal Pharmaceuticals NY LLC	NADOLOL	20 mg/1	1000 TABLET in 1 BOTTLE (69238-1123-1)
69238-1123-3	69238-1123	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170602	N/A	ANDA	ANDA208832	Amneal Pharmaceuticals NY LLC	NADOLOL	20 mg/1	30 TABLET in 1 BOTTLE (69238-1123-3)
69238-1123-9	69238-1123	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170602	N/A	ANDA	ANDA208832	Amneal Pharmaceuticals NY LLC	NADOLOL	20 mg/1	90 TABLET in 1 BOTTLE (69238-1123-9)
67046-1416-3	67046-1416	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20241112	N/A	ANDA	ANDA208832	Coupler LLC	NADOLOL	20 mg/1	30 TABLET in 1 BLISTER PACK (67046-1416-3)