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=ANDA203253"
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
72162-1693-5 72162-1693 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170404 N/A ANDA ANDA203253 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72162-1693-5)
72162-1694-1 72162-1694 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170404 N/A ANDA ANDA203253 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-1694-1)
42708-101-30 42708-101 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20191018 N/A ANDA ANDA203253 QPharma, Inc. SPIRONOLACTONE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42708-101-30)
63187-841-90 63187-841 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170501 N/A ANDA ANDA203253 Proficient Rx LP SPIRONOLACTONE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-841-90)
63629-2437-1 63629-2437 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170404 N/A ANDA ANDA203253 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (63629-2437-1)
63629-2438-1 63629-2438 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170404 N/A ANDA ANDA203253 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (63629-2438-1)
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