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=ANDA062838"
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
53489-400-01 53489-400 HUMAN PRESCRIPTION DRUG Nystatin nystatin TABLET, FILM COATED ORAL 19881222 N/A ANDA ANDA062838 Sun Pharmaceutical Industries, Inc. NYSTATIN 500000 [USP'U]/1 100 TABLET, FILM COATED in 1 BOTTLE (53489-400-01)
53489-400-02 53489-400 HUMAN PRESCRIPTION DRUG Nystatin nystatin TABLET, FILM COATED ORAL 19881222 N/A ANDA ANDA062838 Sun Pharmaceutical Industries, Inc. NYSTATIN 500000 [USP'U]/1 50 TABLET, FILM COATED in 1 BOTTLE (53489-400-02)
53489-400-03 53489-400 HUMAN PRESCRIPTION DRUG Nystatin nystatin TABLET, FILM COATED ORAL 19881222 N/A ANDA ANDA062838 Sun Pharmaceutical Industries, Inc. NYSTATIN 500000 [USP'U]/1 250 TABLET, FILM COATED in 1 BOTTLE (53489-400-03)
53489-400-05 53489-400 HUMAN PRESCRIPTION DRUG Nystatin nystatin TABLET, FILM COATED ORAL 19881222 N/A ANDA ANDA062838 Sun Pharmaceutical Industries, Inc. NYSTATIN 500000 [USP'U]/1 500 TABLET, FILM COATED in 1 BOTTLE (53489-400-05)
53489-400-10 53489-400 HUMAN PRESCRIPTION DRUG Nystatin nystatin TABLET, FILM COATED ORAL 19881222 N/A ANDA ANDA062838 Sun Pharmaceutical Industries, Inc. NYSTATIN 500000 [USP'U]/1 1000 TABLET, FILM COATED in 1 BOTTLE (53489-400-10)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase