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
71335-2286-2 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)
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)
0527-3280-43 0527-3280 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 25 ug/1 1000 TABLET in 1 BOTTLE (0527-3280-43)
0527-3280-46 0527-3280 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 25 ug/1 90 TABLET in 1 BOTTLE (0527-3280-46)
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)
71335-9763-1 71335-9763 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 150 ug/1 30 TABLET in 1 BOTTLE (71335-9763-1)
71335-9763-2 71335-9763 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 150 ug/1 100 TABLET in 1 BOTTLE (71335-9763-2)
71335-9763-3 71335-9763 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 150 ug/1 90 TABLET in 1 BOTTLE (71335-9763-3)
71335-9763-4 71335-9763 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 150 ug/1 60 TABLET in 1 BOTTLE (71335-9763-4)
0527-3283-46 0527-3283 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 88 ug/1 90 TABLET in 1 BOTTLE (0527-3283-46)
0527-3287-43 0527-3287 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 137 ug/1 1000 TABLET in 1 BOTTLE (0527-3287-43)
0527-3287-46 0527-3287 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 137 ug/1 90 TABLET in 1 BOTTLE (0527-3287-46)
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)
71205-655-30 71205-655 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20220427 N/A NDA AUTHORIZED GENERIC NDA021342 Proficient Rx LP LEVOTHYROXINE SODIUM 75 ug/1 30 TABLET in 1 BOTTLE (71205-655-30)
71205-655-60 71205-655 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20220427 N/A NDA AUTHORIZED GENERIC NDA021342 Proficient Rx LP LEVOTHYROXINE SODIUM 75 ug/1 60 TABLET in 1 BOTTLE (71205-655-60)
71205-655-90 71205-655 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20220427 N/A NDA AUTHORIZED GENERIC NDA021342 Proficient Rx LP LEVOTHYROXINE SODIUM 75 ug/1 90 TABLET in 1 BOTTLE (71205-655-90)
0527-3284-43 0527-3284 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 100 ug/1 1000 TABLET in 1 BOTTLE (0527-3284-43)
0527-3284-46 0527-3284 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 100 ug/1 90 TABLET in 1 BOTTLE (0527-3284-46)
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