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
60793-116-01	60793-116	HUMAN PRESCRIPTION DRUG	Cytomel	liothyronine sodium	TABLET	ORAL	19560508	N/A	NDA	NDA010379	Pfizer Laboratories Div Pfizer Inc	LIOTHYRONINE SODIUM	25 ug/1	100 TABLET in 1 BOTTLE (60793-116-01)
60793-117-01	60793-117	HUMAN PRESCRIPTION DRUG	Cytomel	liothyronine sodium	TABLET	ORAL	19560508	N/A	NDA	NDA010379	Pfizer Laboratories Div Pfizer Inc	LIOTHYRONINE SODIUM	50 ug/1	100 TABLET in 1 BOTTLE (60793-117-01)
60793-115-01	60793-115	HUMAN PRESCRIPTION DRUG	Cytomel	liothyronine sodium	TABLET	ORAL	19560508	N/A	NDA	NDA010379	Pfizer Laboratories Div Pfizer Inc	LIOTHYRONINE SODIUM	5 ug/1	100 TABLET in 1 BOTTLE (60793-115-01)
59762-1208-1	59762-1208	HUMAN PRESCRIPTION DRUG	Liothyronine Sodium	liothyronine sodium	TABLET	ORAL	20190624	N/A	NDA AUTHORIZED GENERIC	NDA010379	Greenstone LLC	LIOTHYRONINE SODIUM	50 ug/1	100 TABLET in 1 BOTTLE (59762-1208-1)
59762-1207-1	59762-1207	HUMAN PRESCRIPTION DRUG	Liothyronine Sodium	liothyronine sodium	TABLET	ORAL	20190624	N/A	NDA AUTHORIZED GENERIC	NDA010379	Greenstone LLC	LIOTHYRONINE SODIUM	25 ug/1	100 TABLET in 1 BOTTLE (59762-1207-1)
59762-1206-1	59762-1206	HUMAN PRESCRIPTION DRUG	Liothyronine Sodium	liothyronine sodium	TABLET	ORAL	20190206	N/A	NDA AUTHORIZED GENERIC	NDA010379	Greenstone LLC	LIOTHYRONINE SODIUM	5 ug/1	100 TABLET in 1 BOTTLE (59762-1206-1)