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
72162-1094-0 72162-1094 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 200 ug/1 1000 TABLET in 1 BOTTLE (72162-1094-0)
0527-3281-43 0527-3281 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 50 ug/1 1000 TABLET in 1 BOTTLE (0527-3281-43)
0527-3281-46 0527-3281 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 50 ug/1 90 TABLET in 1 BOTTLE (0527-3281-46)
0527-3285-43 0527-3285 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 112 ug/1 1000 TABLET in 1 BOTTLE (0527-3285-43)
0527-3285-46 0527-3285 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 112 ug/1 90 TABLET in 1 BOTTLE (0527-3285-46)
0527-3289-43 0527-3289 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 175 ug/1 1000 TABLET in 1 BOTTLE (0527-3289-43)
0527-3289-46 0527-3289 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 175 ug/1 90 TABLET in 1 BOTTLE (0527-3289-46)
71205-512-30 71205-512 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium levothyroxine sodium TABLET ORAL 20201202 N/A NDA AUTHORIZED GENERIC NDA021342 Proficient Rx LP LEVOTHYROXINE SODIUM 25 ug/1 30 TABLET in 1 BOTTLE (71205-512-30)
71205-512-60 71205-512 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium levothyroxine sodium TABLET ORAL 20201202 N/A NDA AUTHORIZED GENERIC NDA021342 Proficient Rx LP LEVOTHYROXINE SODIUM 25 ug/1 60 TABLET in 1 BOTTLE (71205-512-60)
71205-512-90 71205-512 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium levothyroxine sodium TABLET ORAL 20201202 N/A NDA AUTHORIZED GENERIC NDA021342 Proficient Rx LP LEVOTHYROXINE SODIUM 25 ug/1 90 TABLET in 1 BOTTLE (71205-512-90)
67046-1612-3 67046-1612 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20251107 N/A NDA AUTHORIZED GENERIC NDA021342 Coupler LLC LEVOTHYROXINE SODIUM 125 ug/1 30 TABLET in 1 BLISTER PACK (67046-1612-3)
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