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=ANDA091382"
符合检索条件的记录共 15 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
62756-589-83 62756-589 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 5 ug/1 30 TABLET in 1 BOTTLE (62756-589-83)
62756-589-88 62756-589 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 5 ug/1 100 TABLET in 1 BOTTLE (62756-589-88)
62756-590-01 62756-590 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20230626 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 25 ug/1 90 TABLET in 1 BOTTLE (62756-590-01)
62756-590-08 62756-590 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 25 ug/1 100 TABLET in 1 BOTTLE (62756-590-08)
62756-590-18 62756-590 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 25 ug/1 1000 TABLET in 1 BOTTLE (62756-590-18)
62756-590-83 62756-590 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 25 ug/1 30 TABLET in 1 BOTTLE (62756-590-83)
62756-590-88 62756-590 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 25 ug/1 100 TABLET in 1 BOTTLE (62756-590-88)
62756-591-01 62756-591 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20230626 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 50 ug/1 90 TABLET in 1 BOTTLE (62756-591-01)
62756-591-08 62756-591 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 50 ug/1 100 TABLET in 1 BOTTLE (62756-591-08)
62756-591-18 62756-591 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 50 ug/1 1000 TABLET in 1 BOTTLE (62756-591-18)
62756-591-83 62756-591 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 50 ug/1 30 TABLET in 1 BOTTLE (62756-591-83)
62756-591-88 62756-591 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 50 ug/1 100 TABLET in 1 BOTTLE (62756-591-88)
62756-589-18 62756-589 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 5 ug/1 1000 TABLET in 1 BOTTLE (62756-589-18)
62756-589-08 62756-589 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20191128 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 5 ug/1 100 TABLET in 1 BOTTLE (62756-589-08)
62756-589-01 62756-589 HUMAN PRESCRIPTION DRUG liothyronine sodium liothyronine sodium TABLET ORAL 20230626 N/A ANDA ANDA091382 Sun Pharmaceutical Industries, Inc. LIOTHYRONINE SODIUM 5 ug/1 90 TABLET in 1 BOTTLE (62756-589-01)
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