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
50268-584-13	50268-584	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20170914	N/A	ANDA	ANDA203578	AvPAK	NIACIN	500 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-584-13) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-584-11)
65162-323-03	65162-323	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20150727	N/A	ANDA	ANDA203578	Amneal Pharmaceuticals LLC	NIACIN	1000 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-323-03)
65162-323-09	65162-323	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20150727	N/A	ANDA	ANDA203578	Amneal Pharmaceuticals LLC	NIACIN	1000 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-323-09)
65162-323-50	65162-323	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20150727	N/A	ANDA	ANDA203578	Amneal Pharmaceuticals LLC	NIACIN	1000 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-323-50)
65162-321-50	65162-321	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20150727	N/A	ANDA	ANDA203578	Amneal Pharmaceuticals LLC	NIACIN	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-321-50)
65162-321-09	65162-321	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20150727	N/A	ANDA	ANDA203578	Amneal Pharmaceuticals LLC	NIACIN	500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-321-09)
65162-321-03	65162-321	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20150727	N/A	ANDA	ANDA203578	Amneal Pharmaceuticals LLC	NIACIN	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-321-03)