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
50090-6573-0	50090-6573	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20230801	N/A	NDA AUTHORIZED GENERIC	NDA021342	A-S Medication Solutions	LEVOTHYROXINE SODIUM	100 ug/1	90 TABLET in 1 BOTTLE (50090-6573-0)
63187-851-30	63187-851	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20170601	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	150 ug/1	30 TABLET in 1 BOTTLE (63187-851-30)
63187-851-60	63187-851	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20170601	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	150 ug/1	60 TABLET in 1 BOTTLE (63187-851-60)
63187-851-90	63187-851	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20170601	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	150 ug/1	90 TABLET in 1 BOTTLE (63187-851-90)
50090-6594-0	50090-6594	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20230818	N/A	NDA AUTHORIZED GENERIC	NDA021342	A-S Medication Solutions	LEVOTHYROXINE SODIUM	50 ug/1	90 TABLET in 1 BOTTLE (50090-6594-0)
71205-232-30	71205-232	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20190301	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	125 ug/1	30 TABLET in 1 BOTTLE (71205-232-30)
71205-232-60	71205-232	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20190301	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	125 ug/1	60 TABLET in 1 BOTTLE (71205-232-60)
71205-232-90	71205-232	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20190301	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	125 ug/1	90 TABLET in 1 BOTTLE (71205-232-90)
63187-924-30	63187-924	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20171101	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	50 ug/1	30 TABLET in 1 BOTTLE (63187-924-30)
63187-924-60	63187-924	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20171101	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	50 ug/1	90 TABLET in 1 BOTTLE (63187-924-60)
63187-924-90	63187-924	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20171101	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	50 ug/1	60 TABLET in 1 BOTTLE (63187-924-90)
63187-982-30	63187-982	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20180201	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	75 ug/1	30 TABLET in 1 BOTTLE (63187-982-30)
63187-982-60	63187-982	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20180201	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	75 ug/1	60 TABLET in 1 BOTTLE (63187-982-60)
63187-982-90	63187-982	HUMAN PRESCRIPTION DRUG	Levothyroxine sodium	Levothyroxine sodium	TABLET	ORAL	20180201	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	75 ug/1	90 TABLET in 1 BOTTLE (63187-982-90)
50090-6831-0	50090-6831	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20231121	N/A	NDA AUTHORIZED GENERIC	NDA021342	A-S Medication Solutions	LEVOTHYROXINE SODIUM	25 ug/1	90 TABLET in 1 BOTTLE (50090-6831-0)
71205-382-30	71205-382	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20200108	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	25 ug/1	30 TABLET in 1 BOTTLE (71205-382-30)
71205-382-60	71205-382	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20200108	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	25 ug/1	60 TABLET in 1 BOTTLE (71205-382-60)
71205-382-90	71205-382	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	Levothyroxine Sodium	TABLET	ORAL	20200108	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	25 ug/1	90 TABLET in 1 BOTTLE (71205-382-90)
71205-512-30	71205-512	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	levothyroxine sodium	TABLET	ORAL	20201202	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	25 ug/1	30 TABLET in 1 BOTTLE (71205-512-30)
71205-512-60	71205-512	HUMAN PRESCRIPTION DRUG	Levothyroxine Sodium	levothyroxine sodium	TABLET	ORAL	20201202	N/A	NDA AUTHORIZED GENERIC	NDA021342	Proficient Rx LP	LEVOTHYROXINE SODIUM	25 ug/1	60 TABLET in 1 BOTTLE (71205-512-60)