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
75907-001-01	75907-001	HUMAN PRESCRIPTION DRUG	Liothyronine Sodium	Liothyronine Sodium	TABLET	ORAL	20240315	N/A	ANDA	ANDA090097	Dr. Reddy's Labratories Inc.	LIOTHYRONINE SODIUM	25 ug/1	100 TABLET in 1 BOTTLE, PLASTIC (75907-001-01)
75907-004-01	75907-004	HUMAN PRESCRIPTION DRUG	Liothyronine Sodium	Liothyronine Sodium	TABLET	ORAL	20240315	N/A	ANDA	ANDA090097	Dr. Reddy's Labratories Inc.	LIOTHYRONINE SODIUM	50 ug/1	100 TABLET in 1 BOTTLE, PLASTIC (75907-004-01)
75907-039-01	75907-039	HUMAN PRESCRIPTION DRUG	Liothyronine Sodium	Liothyronine Sodium	TABLET	ORAL	20240315	N/A	ANDA	ANDA090097	Dr. Reddy's Labratories Inc.	LIOTHYRONINE SODIUM	5 ug/1	100 TABLET in 1 BOTTLE, PLASTIC (75907-039-01)
51862-320-01	51862-320	HUMAN PRESCRIPTION DRUG	Liothyronine Sodium	Liothyronine Sodium	TABLET	ORAL	20180101	N/A	ANDA	ANDA090097	Mayne Pharma Commercial LLC	LIOTHYRONINE SODIUM	5 ug/1	100 TABLET in 1 BOTTLE, PLASTIC (51862-320-01)
51862-321-01	51862-321	HUMAN PRESCRIPTION DRUG	Liothyronine Sodium	Liothyronine Sodium	TABLET	ORAL	20180101	N/A	ANDA	ANDA090097	Mayne Pharma Commercial LLC	LIOTHYRONINE SODIUM	25 ug/1	100 TABLET in 1 BOTTLE, PLASTIC (51862-321-01)
51862-322-01	51862-322	HUMAN PRESCRIPTION DRUG	Liothyronine Sodium	Liothyronine Sodium	TABLET	ORAL	20180101	N/A	ANDA	ANDA090097	Mayne Pharma Commercial LLC	LIOTHYRONINE SODIUM	50 ug/1	100 TABLET in 1 BOTTLE, PLASTIC (51862-322-01)
51407-384-01	51407-384	HUMAN PRESCRIPTION DRUG	Liothyronine Sodium	Liothyronine Sodium	TABLET	ORAL	20200730	N/A	ANDA	ANDA090097	Golden State Medical Supply, Inc.	LIOTHYRONINE SODIUM	5 ug/1	100 TABLET in 1 BOTTLE, PLASTIC (51407-384-01)
51407-385-01	51407-385	HUMAN PRESCRIPTION DRUG	Liothyronine Sodium	Liothyronine Sodium	TABLET	ORAL	20200730	N/A	ANDA	ANDA090097	Golden State Medical Supply, Inc.	LIOTHYRONINE SODIUM	25 ug/1	100 TABLET in 1 BOTTLE, PLASTIC (51407-385-01)