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
50090-7206-0	50090-7206	HUMAN PRESCRIPTION DRUG	Felopdipine	Felodipine	TABLET, EXTENDED RELEASE	ORAL	20240805	N/A	ANDA	ANDA210847	A-S Medication Solutions	FELODIPINE	10 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7206-0)
69367-266-01	69367-266	HUMAN PRESCRIPTION DRUG	Felopdipine	Felodipine	TABLET, EXTENDED RELEASE	ORAL	20230331	N/A	ANDA	ANDA210847	Westminster Pharmaceuticals, LLC	FELODIPINE	10 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-266-01)
69367-264-01	69367-264	HUMAN PRESCRIPTION DRUG	Felodipine	Felodipine	TABLET, EXTENDED RELEASE	ORAL	20230331	N/A	ANDA	ANDA210847	Westminster Pharmaceuticals, LLC	FELODIPINE	2.5 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-264-01)
69117-0030-1	69117-0030	HUMAN PRESCRIPTION DRUG	Felodipine	Felodipine Extended-release Tablets	TABLET, EXTENDED RELEASE	ORAL	20190801	N/A	ANDA	ANDA210847	Yiling Pharmaceutical Inc.	FELODIPINE	10 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0030-1)
69117-0030-2	69117-0030	HUMAN PRESCRIPTION DRUG	Felodipine	Felodipine Extended-release Tablets	TABLET, EXTENDED RELEASE	ORAL	20190801	N/A	ANDA	ANDA210847	Yiling Pharmaceutical Inc.	FELODIPINE	10 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0030-2)
62135-647-90	62135-647	HUMAN PRESCRIPTION DRUG	Felodipine	Felodipine	TABLET, EXTENDED RELEASE	ORAL	20230605	N/A	ANDA	ANDA210847	Chartwell RX, LLC	FELODIPINE	5 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-647-90)
69117-0028-1	69117-0028	HUMAN PRESCRIPTION DRUG	Felodipine	Felodipine Extended-release Tablets	TABLET, EXTENDED RELEASE	ORAL	20190801	N/A	ANDA	ANDA210847	Yiling Pharmaceutical Inc.	FELODIPINE	2.5 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0028-1)
69117-0028-2	69117-0028	HUMAN PRESCRIPTION DRUG	Felodipine	Felodipine Extended-release Tablets	TABLET, EXTENDED RELEASE	ORAL	20190801	N/A	ANDA	ANDA210847	Yiling Pharmaceutical Inc.	FELODIPINE	2.5 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0028-2)
69117-0029-1	69117-0029	HUMAN PRESCRIPTION DRUG	Felodipine	Felodipine Extended-release Tablets	TABLET, EXTENDED RELEASE	ORAL	20190801	N/A	ANDA	ANDA210847	Yiling Pharmaceutical Inc.	FELODIPINE	5 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0029-1)
69117-0029-2	69117-0029	HUMAN PRESCRIPTION DRUG	Felodipine	Felodipine Extended-release Tablets	TABLET, EXTENDED RELEASE	ORAL	20190801	N/A	ANDA	ANDA210847	Yiling Pharmaceutical Inc.	FELODIPINE	5 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0029-2)
62135-646-90	62135-646	HUMAN PRESCRIPTION DRUG	Felodipine	Felodipine	TABLET, EXTENDED RELEASE	ORAL	20230605	N/A	ANDA	ANDA210847	Chartwell RX, LLC	FELODIPINE	2.5 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-646-90)
69367-265-01	69367-265	HUMAN PRESCRIPTION DRUG	Felodipine	Felodipine	TABLET, EXTENDED RELEASE	ORAL	20230331	N/A	ANDA	ANDA210847	Westminster Pharmaceuticals, LLC	FELODIPINE	5 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-265-01)
62135-648-90	62135-648	HUMAN PRESCRIPTION DRUG	Felodipine	Felodipine	TABLET, EXTENDED RELEASE	ORAL	20230605	N/A	ANDA	ANDA210847	Chartwell RX, LLC	FELODIPINE	10 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-648-90)