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=NDA021342"
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
71335-1625-4 71335-1625 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240403 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 25 ug/1 60 TABLET in 1 BOTTLE (71335-1625-4)
71335-1625-5 71335-1625 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240403 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 25 ug/1 28 TABLET in 1 BOTTLE (71335-1625-5)
71335-1625-6 71335-1625 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240403 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 25 ug/1 10 TABLET in 1 BOTTLE (71335-1625-6)
71335-2286-1 71335-2286 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240403 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 200 ug/1 1000 TABLET in 1 BOTTLE (71335-2286-1)
71335-2286-2 71335-2286 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240403 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 200 ug/1 30 TABLET in 1 BOTTLE (71335-2286-2)
72162-1091-0 72162-1091 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 112 ug/1 1000 TABLET in 1 BOTTLE (72162-1091-0)
72162-1095-0 72162-1095 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240206 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 300 ug/1 1000 TABLET in 1 BOTTLE (72162-1095-0)
63629-2090-1 63629-2090 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20210209 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 175 ug/1 1000 TABLET in 1 BOTTLE (63629-2090-1)
71335-1955-5 71335-1955 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20210928 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 112 ug/1 100 TABLET in 1 BOTTLE (71335-1955-5)
82804-099-30 82804-099 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240425 N/A NDA AUTHORIZED GENERIC NDA021342 Proficient Rx LP LEVOTHYROXINE SODIUM 50 ug/1 30 TABLET in 1 BOTTLE (82804-099-30)
82804-099-90 82804-099 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240501 N/A NDA AUTHORIZED GENERIC NDA021342 Proficient Rx LP LEVOTHYROXINE SODIUM 50 ug/1 90 TABLET in 1 BOTTLE (82804-099-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase