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
0378-2099-01	0378-2099	HUMAN PRESCRIPTION DRUG	Nisoldipine	nisoldipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110128	N/A	ANDA	ANDA091001	Mylan Pharmaceuticals Inc.	NISOLDIPINE	34 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2099-01)
0378-2098-01	0378-2098	HUMAN PRESCRIPTION DRUG	Nisoldipine	nisoldipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110128	N/A	ANDA	ANDA091001	Mylan Pharmaceuticals Inc.	NISOLDIPINE	25.5 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2098-01)
0378-2097-01	0378-2097	HUMAN PRESCRIPTION DRUG	Nisoldipine	nisoldipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110128	N/A	ANDA	ANDA091001	Mylan Pharmaceuticals Inc.	NISOLDIPINE	17 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2097-01)
0378-2096-01	0378-2096	HUMAN PRESCRIPTION DRUG	Nisoldipine	nisoldipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110128	N/A	ANDA	ANDA091001	Mylan Pharmaceuticals Inc.	NISOLDIPINE	8.5 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2096-01)