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
51407-267-90	51407-267	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20190705	N/A	ANDA	ANDA203899	Golden State Medical Supply, Inc.	NIACIN	500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (51407-267-90)
51407-268-90	51407-268	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20190705	N/A	ANDA	ANDA203899	Golden State Medical Supply, Inc.	NIACIN	1000 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (51407-268-90)
62135-497-90	62135-497	HUMAN PRESCRIPTION DRUG	NIACIN	Niacin	TABLET, EXTENDED RELEASE	ORAL	20230308	N/A	ANDA	ANDA203899	Chartwell RX, LLC	NIACIN	500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-497-90)
62135-498-90	62135-498	HUMAN PRESCRIPTION DRUG	NIACIN	Niacin	TABLET, EXTENDED RELEASE	ORAL	20230308	N/A	ANDA	ANDA203899	Chartwell RX, LLC	NIACIN	1000 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-498-90)
62175-320-43	62175-320	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20170216	N/A	ANDA	ANDA203899	Lannett Company, Inc.	NIACIN	500 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-320-43)
62175-320-46	62175-320	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20170216	N/A	ANDA	ANDA203899	Lannett Company, Inc.	NIACIN	500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-320-46)
62175-322-43	62175-322	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20170216	N/A	ANDA	ANDA203899	Lannett Company, Inc.	NIACIN	1000 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-322-43)
62175-322-46	62175-322	HUMAN PRESCRIPTION DRUG	Niacin	Niacin	TABLET, EXTENDED RELEASE	ORAL	20170216	N/A	ANDA	ANDA203899	Lannett Company, Inc.	NIACIN	1000 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-322-46)