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
51655-583-52	51655-583	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20230330	N/A	NDA AUTHORIZED GENERIC	NDA021342	Northwind Pharmaceuticals, LLC	LEVOTHYROXINE SODIUM	150 ug/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-583-52)
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)
51655-578-52	51655-578	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20230329	N/A	NDA AUTHORIZED GENERIC	NDA021342	Northwind Pharmaceuticals, LLC	LEVOTHYROXINE SODIUM	200 ug/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-578-52)
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)
68071-2278-9	68071-2278	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20201015	N/A	NDA AUTHORIZED GENERIC	NDA021342	NuCare Pharmaceuticals,Inc.	LEVOTHYROXINE SODIUM	100 ug/1	90 TABLET in 1 BOTTLE (68071-2278-9)