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
0781-8017-01	0781-8017	HUMAN PRESCRIPTION DRUG	FLUVASTATIN SODIUM ER	fluvastatin sodium	TABLET, EXTENDED RELEASE	ORAL	20180502	N/A	NDA AUTHORIZED GENERIC	NDA021192	Sandoz Inc	FLUVASTATIN SODIUM	80 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-8017-01)
0781-8017-31	0781-8017	HUMAN PRESCRIPTION DRUG	FLUVASTATIN SODIUM ER	fluvastatin sodium	TABLET, EXTENDED RELEASE	ORAL	20180502	N/A	NDA AUTHORIZED GENERIC	NDA021192	Sandoz Inc	FLUVASTATIN SODIUM	80 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-8017-31)
0078-0354-15	0078-0354	HUMAN PRESCRIPTION DRUG	Lescol XL	fluvastatin sodium	TABLET, EXTENDED RELEASE	ORAL	20001006	N/A	NDA	NDA021192	Novartis Pharmaceuticals Corporation	FLUVASTATIN SODIUM	80 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0078-0354-15)
66758-211-31	66758-211	HUMAN PRESCRIPTION DRUG	Lescol XL	fluvastatin sodium	TABLET, EXTENDED RELEASE	ORAL	20240802	N/A	NDA	NDA021192	Sandoz Inc	FLUVASTATIN SODIUM	80 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (66758-211-31)