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
51655-432-52	51655-432	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200909	N/A	ANDA	ANDA079057	Northwind Pharmaceuticals, LLC	ALFUZOSIN HYDROCHLORIDE	10 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-432-52)
72162-1449-9	72162-1449	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240716	N/A	ANDA	ANDA079057	Bryant Ranch Prepack	ALFUZOSIN HYDROCHLORIDE	10 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1449-9)
47335-956-08	47335-956	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20111122	N/A	ANDA	ANDA079057	Sun Pharmaceutical Industries, Inc.	ALFUZOSIN HYDROCHLORIDE	10 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08)
47335-956-18	47335-956	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20111122	N/A	ANDA	ANDA079057	Sun Pharmaceutical Industries, Inc.	ALFUZOSIN HYDROCHLORIDE	10 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18)
47335-956-81	47335-956	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20111122	N/A	ANDA	ANDA079057	Sun Pharmaceutical Industries, Inc.	ALFUZOSIN HYDROCHLORIDE	10 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-81)
47335-956-83	47335-956	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20111122	N/A	ANDA	ANDA079057	Sun Pharmaceutical Industries, Inc.	ALFUZOSIN HYDROCHLORIDE	10 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-83)
47335-956-88	47335-956	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20111122	N/A	ANDA	ANDA079057	Sun Pharmaceutical Industries, Inc.	ALFUZOSIN HYDROCHLORIDE	10 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88)
71335-2146-4	71335-2146	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA079057	Bryant Ranch Prepack	ALFUZOSIN HYDROCHLORIDE	10 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-4)
71335-2146-5	71335-2146	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA079057	Bryant Ranch Prepack	ALFUZOSIN HYDROCHLORIDE	10 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-5)
71335-2146-1	71335-2146	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA079057	Bryant Ranch Prepack	ALFUZOSIN HYDROCHLORIDE	10 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-1)
71335-2146-2	71335-2146	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA079057	Bryant Ranch Prepack	ALFUZOSIN HYDROCHLORIDE	10 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-2)
71335-2146-3	71335-2146	HUMAN PRESCRIPTION DRUG	Alfuzosin Hydrochloride	Alfuzosin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230130	N/A	ANDA	ANDA079057	Bryant Ranch Prepack	ALFUZOSIN HYDROCHLORIDE	10 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-3)