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)
检索条件:" 注册申请号=ANDA079060"
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
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)
71335-2578-1 71335-2578 HUMAN PRESCRIPTION DRUG Alfuzosin Hydrochloride Alfuzosin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250206 N/A ANDA ANDA079060 Bryant Ranch Prepack ALFUZOSIN HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-1)
71335-2578-2 71335-2578 HUMAN PRESCRIPTION DRUG Alfuzosin Hydrochloride Alfuzosin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250206 N/A ANDA ANDA079060 Bryant Ranch Prepack ALFUZOSIN HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-2)
71335-2578-3 71335-2578 HUMAN PRESCRIPTION DRUG Alfuzosin Hydrochloride Alfuzosin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250206 N/A ANDA ANDA079060 Bryant Ranch Prepack ALFUZOSIN HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-3)
71335-2578-4 71335-2578 HUMAN PRESCRIPTION DRUG Alfuzosin Hydrochloride Alfuzosin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250206 N/A ANDA ANDA079060 Bryant Ranch Prepack ALFUZOSIN HYDROCHLORIDE 10 mg/1 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-4)
71335-2578-5 71335-2578 HUMAN PRESCRIPTION DRUG Alfuzosin Hydrochloride Alfuzosin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250206 N/A ANDA ANDA079060 Bryant Ranch Prepack ALFUZOSIN HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-5)
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)
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