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
60846-803-01	60846-803	HUMAN PRESCRIPTION DRUG	Unithroid	levothyroxine sodium	TABLET	ORAL	20140703	N/A	NDA	NDA021210	Amneal Pharmaceuticals LLC	LEVOTHYROXINE SODIUM	75 ug/1	100 TABLET in 1 BOTTLE (60846-803-01)
60846-807-01	60846-807	HUMAN PRESCRIPTION DRUG	Unithroid	levothyroxine sodium	TABLET	ORAL	20140703	N/A	NDA	NDA021210	Amneal Pharmaceuticals LLC	LEVOTHYROXINE SODIUM	125 ug/1	100 TABLET in 1 BOTTLE (60846-807-01)
60846-812-01	60846-812	HUMAN PRESCRIPTION DRUG	Unithroid	levothyroxine sodium	TABLET	ORAL	20140703	N/A	NDA	NDA021210	Amneal Pharmaceuticals LLC	LEVOTHYROXINE SODIUM	300 ug/1	100 TABLET in 1 BOTTLE (60846-812-01)
71205-221-30	71205-221	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20031201	N/A	NDA	NDA021210	Proficient Rx LP	LEVOTHYROXINE SODIUM	.025 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (71205-221-30)
71205-221-60	71205-221	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20031201	N/A	NDA	NDA021210	Proficient Rx LP	LEVOTHYROXINE SODIUM	.025 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (71205-221-60)
71205-221-90	71205-221	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20190201	N/A	NDA	NDA021210	Proficient Rx LP	LEVOTHYROXINE SODIUM	.025 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (71205-221-90)