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
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)
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)
0527-3288-46 0527-3288 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 150 ug/1 90 TABLET in 1 BOTTLE (0527-3288-46)
71335-2039-1 71335-2039 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240528 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 75 ug/1 30 TABLET in 1 BOTTLE (71335-2039-1)
71335-2039-2 71335-2039 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240528 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 75 ug/1 100 TABLET in 1 BOTTLE (71335-2039-2)
71335-2039-3 71335-2039 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240528 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 75 ug/1 60 TABLET in 1 BOTTLE (71335-2039-3)
71335-2039-4 71335-2039 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240528 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 75 ug/1 90 TABLET in 1 BOTTLE (71335-2039-4)
71335-2039-5 71335-2039 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240528 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 75 ug/1 28 TABLET in 1 BOTTLE (71335-2039-5)
71335-2039-6 71335-2039 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20240528 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 75 ug/1 10 TABLET in 1 BOTTLE (71335-2039-6)
63629-2088-1 63629-2088 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20210209 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 112 ug/1 1000 TABLET in 1 BOTTLE (63629-2088-1)
63629-2092-1 63629-2092 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20210209 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 88 ug/1 1000 TABLET in 1 BOTTLE (63629-2092-1)
51655-537-52 51655-537 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20221228 N/A NDA AUTHORIZED GENERIC NDA021342 Northwind Pharmaceuticals, LLC LEVOTHYROXINE SODIUM 175 ug/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-537-52)
51655-576-52 51655-576 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20221227 N/A NDA AUTHORIZED GENERIC NDA021342 Northwind Pharmaceuticals, LLC LEVOTHYROXINE SODIUM 75 ug/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-576-52)
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)
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)
51655-128-52 51655-128 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20230306 N/A NDA AUTHORIZED GENERIC NDA021342 Northwind Pharmaceuticals, LLC LEVOTHYROXINE SODIUM 137 ug/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-128-52)
71335-1625-1 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 30 TABLET in 1 BOTTLE (71335-1625-1)
51655-579-52 51655-579 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20221228 N/A NDA AUTHORIZED GENERIC NDA021342 Northwind Pharmaceuticals, LLC LEVOTHYROXINE SODIUM 112 ug/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-579-52)
51655-728-52 51655-728 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20210616 N/A NDA AUTHORIZED GENERIC NDA021342 Northwind Pharmaceuticals, LLC LEVOTHYROXINE SODIUM 88 ug/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-728-52)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase