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
0555-0483-02	0555-0483	HUMAN PRESCRIPTION DRUG	Amiloride Hydrochloride and Hydrochlorothiazide	Amiloride Hydrochloride and Hydrochlorothiazide	TABLET	ORAL	19891201	N/A	ANDA	ANDA071111	Teva Pharmaceuticals USA, Inc.	AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	5 mg/1; 50 mg/1	100 TABLET in 1 BOTTLE (0555-0483-02)
0555-0483-05	0555-0483	HUMAN PRESCRIPTION DRUG	Amiloride Hydrochloride and Hydrochlorothiazide	Amiloride Hydrochloride and Hydrochlorothiazide	TABLET	ORAL	19891201	N/A	ANDA	ANDA071111	Teva Pharmaceuticals USA, Inc.	AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	5 mg/1; 50 mg/1	1000 TABLET in 1 BOTTLE (0555-0483-05)
50090-0513-1	50090-0513	HUMAN PRESCRIPTION DRUG	Amiloride Hydrochloride and Hydrochlorothiazide	Amiloride Hydrochloride and Hydrochlorothiazide	TABLET	ORAL	20160629	N/A	ANDA	ANDA071111	A-S Medication Solutions	AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	5 mg/1; 50 mg/1	30 TABLET in 1 BOTTLE (50090-0513-1)
50090-0513-0	50090-0513	HUMAN PRESCRIPTION DRUG	Amiloride Hydrochloride and Hydrochlorothiazide	Amiloride Hydrochloride and Hydrochlorothiazide	TABLET	ORAL	20141128	N/A	ANDA	ANDA071111	A-S Medication Solutions	AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	5 mg/1; 50 mg/1	28 TABLET in 1 BOTTLE (50090-0513-0)