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）

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
0480-8682-10	0480-8682	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20220921	20260831	ANDA	ANDA207588	Teva Pharmaceuticals, Inc.	LEVOTHYROXINE SODIUM	25 ug/1	1000 TABLET in 1 BOTTLE (0480-8682-10)
0480-8682-98	0480-8682	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20220921	20260831	ANDA	ANDA207588	Teva Pharmaceuticals, Inc.	LEVOTHYROXINE SODIUM	25 ug/1	90 TABLET in 1 BOTTLE (0480-8682-98)
0480-8687-10	0480-8687	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20220921	20260930	ANDA	ANDA207588	Teva Pharmaceuticals, Inc.	LEVOTHYROXINE SODIUM	50 ug/1	1000 TABLET in 1 BOTTLE (0480-8687-10)
0480-8687-98	0480-8687	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20220921	20260930	ANDA	ANDA207588	Teva Pharmaceuticals, Inc.	LEVOTHYROXINE SODIUM	50 ug/1	90 TABLET in 1 BOTTLE (0480-8687-98)
0480-8693-10	0480-8693	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20220921	20261130	ANDA	ANDA207588	Teva Pharmaceuticals, Inc.	LEVOTHYROXINE SODIUM	88 ug/1	1000 TABLET in 1 BOTTLE (0480-8693-10)
0480-8693-98	0480-8693	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20220921	20261130	ANDA	ANDA207588	Teva Pharmaceuticals, Inc.	LEVOTHYROXINE SODIUM	88 ug/1	90 TABLET in 1 BOTTLE (0480-8693-98)