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
70515-500-10	70515-500	HUMAN PRESCRIPTION DRUG	Sular	nisoldipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170203	N/A	NDA	NDA020356	Covis Pharma US, Inc	NISOLDIPINE	8.5 mg/1	1 BOTTLE in 1 CARTON (70515-500-10) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
70515-501-10	70515-501	HUMAN PRESCRIPTION DRUG	Sular	nisoldipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170203	N/A	NDA	NDA020356	Covis Pharma US, Inc	NISOLDIPINE	17 mg/1	1 BOTTLE in 1 CARTON (70515-501-10) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
70515-503-10	70515-503	HUMAN PRESCRIPTION DRUG	Sular	nisoldipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170203	N/A	NDA	NDA020356	Covis Pharma US, Inc	NISOLDIPINE	34 mg/1	1 BOTTLE in 1 CARTON (70515-503-10) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
66993-472-02	66993-472	HUMAN PRESCRIPTION DRUG	Nisoldipine	Nisoldipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120227	N/A	NDA AUTHORIZED GENERIC	NDA020356	Prasco Laboratories	NISOLDIPINE	8.5 mg/1	1 BOTTLE in 1 CARTON (66993-472-02) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
66993-473-02	66993-473	HUMAN PRESCRIPTION DRUG	Nisoldipine	Nisoldipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120227	N/A	NDA AUTHORIZED GENERIC	NDA020356	Prasco Laboratories	NISOLDIPINE	17 mg/1	1 BOTTLE in 1 CARTON (66993-473-02) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
66993-475-02	66993-475	HUMAN PRESCRIPTION DRUG	Nisoldipine	Nisoldipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120227	N/A	NDA AUTHORIZED GENERIC	NDA020356	Prasco Laboratories	NISOLDIPINE	34 mg/1	1 BOTTLE in 1 CARTON (66993-475-02) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE