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
63629-9450-1	63629-9450	HUMAN PRESCRIPTION DRUG	Dalfampridine	Dalfampridine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220928	N/A	ANDA	ANDA206765	Bryant Ranch Prepack	DALFAMPRIDINE	10 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9450-1)
51407-876-60	51407-876	HUMAN PRESCRIPTION DRUG	Dalfampridine	Dalfampridine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240205	N/A	ANDA	ANDA206765	Golden State Medical Supply, Inc.	DALFAMPRIDINE	10 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51407-876-60)
67877-444-05	67877-444	HUMAN PRESCRIPTION DRUG	Dalfampridine	Dalfampridine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180731	N/A	ANDA	ANDA206765	Ascend Laboratories, LLC	DALFAMPRIDINE	10 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-444-05)
67877-444-60	67877-444	HUMAN PRESCRIPTION DRUG	Dalfampridine	Dalfampridine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180731	N/A	ANDA	ANDA206765	Ascend Laboratories, LLC	DALFAMPRIDINE	10 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-444-60)
67877-444-90	67877-444	HUMAN PRESCRIPTION DRUG	Dalfampridine	Dalfampridine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180731	N/A	ANDA	ANDA206765	Ascend Laboratories, LLC	DALFAMPRIDINE	10 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-444-90)