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
68788-7969-3	68788-7969	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine Sodium	TABLET	ORAL	20210728	N/A	ANDA	ANDA212399	Preferred Pharmaceuticals Inc.	LEVOTHYROXINE SODIUM	25 ug/1	30 TABLET in 1 BOTTLE (68788-7969-3)
68788-7969-9	68788-7969	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine Sodium	TABLET	ORAL	20210728	N/A	ANDA	ANDA212399	Preferred Pharmaceuticals Inc.	LEVOTHYROXINE SODIUM	25 ug/1	90 TABLET in 1 BOTTLE (68788-7969-9)
70518-3208-0	70518-3208	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine Sodium	TABLET	ORAL	20220807	N/A	ANDA	ANDA212399	REMEDYREPACK INC.	LEVOTHYROXINE SODIUM	50 ug/1	90 TABLET in 1 BOTTLE (70518-3208-0)
72789-297-30	72789-297	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine Sodium	TABLET	ORAL	20230111	N/A	ANDA	ANDA212399	PD-Rx Pharmaceuticals, Inc.	LEVOTHYROXINE SODIUM	100 ug/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-297-30)
82804-168-30	82804-168	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine Sodium	TABLET	ORAL	20241209	N/A	ANDA	ANDA212399	Proficient Rx LP	LEVOTHYROXINE SODIUM	25 ug/1	30 TABLET in 1 BOTTLE (82804-168-30)
82804-168-90	82804-168	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine Sodium	TABLET	ORAL	20241223	N/A	ANDA	ANDA212399	Proficient Rx LP	LEVOTHYROXINE SODIUM	25 ug/1	90 TABLET in 1 BOTTLE (82804-168-90)
67296-2048-3	67296-2048	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine Sodium	TABLET	ORAL	20201210	N/A	ANDA	ANDA212399	Redpharm drug	LEVOTHYROXINE SODIUM	100 ug/1	30 TABLET in 1 BOTTLE (67296-2048-3)