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
65862-249-01	65862-249	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120830	N/A	ANDA	ANDA079060	Aurobindo Pharma Limited	ALFUZOSIN HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-01)
65862-249-05	65862-249	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120830	N/A	ANDA	ANDA079060	Aurobindo Pharma Limited	ALFUZOSIN HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-05)
65862-249-30	65862-249	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120830	N/A	ANDA	ANDA079060	Aurobindo Pharma Limited	ALFUZOSIN HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-30)
65862-249-90	65862-249	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120830	N/A	ANDA	ANDA079060	Aurobindo Pharma Limited	ALFUZOSIN HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-90)
65862-249-99	65862-249	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120830	N/A	ANDA	ANDA079060	Aurobindo Pharma Limited	ALFUZOSIN HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-99)
57237-114-01	57237-114	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120830	N/A	ANDA	ANDA079060	Rising Pharma Holdings, Inc.	ALFUZOSIN HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-01)
57237-114-05	57237-114	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120830	N/A	ANDA	ANDA079060	Rising Pharma Holdings, Inc.	ALFUZOSIN HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-05)
57237-114-90	57237-114	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20120830	N/A	ANDA	ANDA079060	Rising Pharma Holdings, Inc.	ALFUZOSIN HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-90)
51655-087-52	51655-087	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221004	N/A	ANDA	ANDA079060	Northwind Pharmaceuticals, LLC	ALFUZOSIN HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-087-52)