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
71741-020-90	71741-020	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET	ORAL	20211216	N/A	ANDA	ANDA040378	Redmont Pharmaceuticals, LLC	NIACIN	500 mg/1	90 TABLET in 1 BOTTLE (71741-020-90)
71741-047-90	71741-047	HUMAN PRESCRIPTION DRUG	NIACIN	NIACIN	TABLET	ORAL	20190429	N/A	ANDA	ANDA040378	Redmont Pharmaceuticals, LLC	NIACIN	500 mg/1	90 TABLET in 1 BOTTLE (71741-047-90)
72919-420-90	72919-420	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET	ORAL	20210331	N/A	ANDA	ANDA040378	Emerald Therapeutics, LLC	NIACIN	500 mg/1	90 TABLET in 1 BOTTLE (72919-420-90)
71740-201-10	71740-201	HUMAN PRESCRIPTION DRUG	Niacor	niacin	TABLET	ORAL	20171113	N/A	ANDA	ANDA040378	Avondale Pharmaceuticals, LLC	NIACIN	500 mg/1	100 TABLET in 1 BOTTLE (71740-201-10)
71740-001-10	71740-001	HUMAN PRESCRIPTION DRUG	Niacor	Niacin	TABLET	ORAL	20211216	N/A	ANDA	ANDA040378	Avondale Pharmaceuticals, LLC	NIACIN	500 mg/1	100 TABLET in 1 BOTTLE (71740-001-10)