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
46708-448-30	46708-448	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160523	N/A	ANDA	ANDA091617	Alembic Pharmaceuticals Limited	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-448-30)
46708-448-90	46708-448	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160523	N/A	ANDA	ANDA091617	Alembic Pharmaceuticals Limited	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-448-90)
46708-448-91	46708-448	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160523	N/A	ANDA	ANDA091617	Alembic Pharmaceuticals Limited	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (46708-448-91)
63187-394-30	63187-394	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20161003	N/A	ANDA	ANDA091617	Proficient Rx LP	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-394-30)
63187-394-60	63187-394	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20161003	N/A	ANDA	ANDA091617	Proficient Rx LP	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-394-60)
63187-394-90	63187-394	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20161003	N/A	ANDA	ANDA091617	Proficient Rx LP	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-394-90)
68071-4159-3	68071-4159	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171117	N/A	ANDA	ANDA091617	NuCare Pharmaceuticals,Inc.	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	12.5 mg/1; 100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-4159-3)
62332-050-10	62332-050	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160523	N/A	ANDA	ANDA091617	Alembic Pharmaceuticals Inc.	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	25 mg/1; 100 mg/1	100 BLISTER PACK in 1 CARTON (62332-050-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
62332-050-30	62332-050	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160523	N/A	ANDA	ANDA091617	Alembic Pharmaceuticals Inc.	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	25 mg/1; 100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-050-30)
62332-050-90	62332-050	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160523	N/A	ANDA	ANDA091617	Alembic Pharmaceuticals Inc.	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	25 mg/1; 100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-050-90)
62332-050-91	62332-050	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20160523	N/A	ANDA	ANDA091617	Alembic Pharmaceuticals Inc.	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	25 mg/1; 100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62332-050-91)