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
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)
51655-544-52 51655-544 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20221227 N/A NDA AUTHORIZED GENERIC NDA021342 Northwind Health Company, LLC LEVOTHYROXINE SODIUM 100 ug/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-544-52)
71335-1814-0 71335-1814 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20211220 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 100 ug/1 1000 TABLET in 1 BOTTLE (71335-1814-0)
71335-1814-1 71335-1814 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20211220 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 100 ug/1 100 TABLET in 1 BOTTLE (71335-1814-1)
71335-1814-2 71335-1814 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20211220 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 100 ug/1 30 TABLET in 1 BOTTLE (71335-1814-2)
71335-1814-3 71335-1814 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20211220 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 100 ug/1 60 TABLET in 1 BOTTLE (71335-1814-3)
71335-1814-4 71335-1814 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20211220 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 100 ug/1 7 TABLET in 1 BOTTLE (71335-1814-4)
71335-1814-5 71335-1814 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20211220 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 100 ug/1 14 TABLET in 1 BOTTLE (71335-1814-5)
71335-1814-6 71335-1814 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20211220 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 100 ug/1 90 TABLET in 1 BOTTLE (71335-1814-6)
71335-1814-7 71335-1814 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20211220 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 100 ug/1 28 TABLET in 1 BOTTLE (71335-1814-7)
71335-1814-8 71335-1814 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20211220 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 100 ug/1 56 TABLET in 1 BOTTLE (71335-1814-8)
63629-2091-1 63629-2091 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20210209 N/A NDA AUTHORIZED GENERIC NDA021342 Bryant Ranch Prepack LEVOTHYROXINE SODIUM 200 ug/1 1000 TABLET in 1 BOTTLE (63629-2091-1)
51655-537-52 51655-537 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20221228 N/A NDA AUTHORIZED GENERIC NDA021342 Northwind Health Company, LLC LEVOTHYROXINE SODIUM 175 ug/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-537-52)
51655-579-52 51655-579 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20221228 N/A NDA AUTHORIZED GENERIC NDA021342 Northwind Health Company, LLC LEVOTHYROXINE SODIUM 112 ug/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-579-52)
55466-105-11 55466-105 HUMAN PRESCRIPTION DRUG LEVO-T Levothyroxine Sodium TABLET ORAL 20151029 N/A NDA NDA021342 Neolpharma, Inc. LEVOTHYROXINE SODIUM 50 ug/1 90 TABLET in 1 BOTTLE (55466-105-11)
55466-105-19 55466-105 HUMAN PRESCRIPTION DRUG LEVO-T Levothyroxine Sodium TABLET ORAL 20180807 N/A NDA NDA021342 Neolpharma, Inc. LEVOTHYROXINE SODIUM 50 ug/1 1000 TABLET in 1 BOTTLE (55466-105-19)
55466-109-11 55466-109 HUMAN PRESCRIPTION DRUG LEVO-T Levothyroxine Sodium TABLET ORAL 20151029 N/A NDA NDA021342 Neolpharma, Inc. LEVOTHYROXINE SODIUM 112 ug/1 90 TABLET in 1 BOTTLE (55466-109-11)
55466-113-11 55466-113 HUMAN PRESCRIPTION DRUG LEVO-T Levothyroxine Sodium TABLET ORAL 20151029 N/A NDA NDA021342 Neolpharma, Inc. LEVOTHYROXINE SODIUM 175 ug/1 90 TABLET in 1 BOTTLE (55466-113-11)
0527-3282-43 0527-3282 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 75 ug/1 1000 TABLET in 1 BOTTLE (0527-3282-43)
0527-3282-46 0527-3282 HUMAN PRESCRIPTION DRUG Levothyroxine Sodium Levothyroxine Sodium TABLET ORAL 20200803 N/A NDA AUTHORIZED GENERIC NDA021342 Lannett Company, Inc LEVOTHYROXINE SODIUM 75 ug/1 90 TABLET in 1 BOTTLE (0527-3282-46)
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