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
0615-7959-05	0615-7959	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20190618	N/A	ANDA	ANDA078243	NCS HealthCare of KY, LLC dba Vangard Labs	LOSARTAN POTASSIUM	50 mg/1	15 TABLET, FILM COATED in 1 BLISTER PACK (0615-7959-05)
0615-7959-28	0615-7959	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20250102	N/A	ANDA	ANDA078243	NCS HealthCare of KY, LLC dba Vangard Labs	LOSARTAN POTASSIUM	50 mg/1	28 TABLET, FILM COATED in 1 BLISTER PACK (0615-7959-28)
0615-7959-39	0615-7959	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20190618	N/A	ANDA	ANDA078243	NCS HealthCare of KY, LLC dba Vangard Labs	LOSARTAN POTASSIUM	50 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7959-39)
50268-504-15	50268-504	HUMAN PRESCRIPTION DRUG	Losortan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20200529	N/A	ANDA	ANDA078243	AvPAK	LOSARTAN POTASSIUM	25 mg/1	50 BLISTER PACK in 1 BOX (50268-504-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-504-11)
55154-2327-0	55154-2327	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Cardinal Health 107, LLC	LOSARTAN POTASSIUM	50 mg/1	10 BLISTER PACK in 1 BAG (55154-2327-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
68084-348-01	68084-348	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101013	N/A	ANDA	ANDA078243	American Health Packaging	LOSARTAN POTASSIUM	100 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-348-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-348-11)
55154-2089-0	55154-2089	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101012	N/A	ANDA	ANDA078243	Cardinal Health 107, LLC	LOSARTAN POTASSIUM	50 mg/1	10 BLISTER PACK in 1 BAG (55154-2089-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
82009-042-10	82009-042	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20220920	N/A	ANDA	ANDA078243	Quallent Pharmaceuticals Health LLC	LOSARTAN POTASSIUM	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (82009-042-10)
0904-7047-61	0904-7047	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Major Pharmaceuticals	LOSARTAN POTASSIUM	25 mg/1	100 BLISTER PACK in 1 CARTON (0904-7047-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
68382-136-01	68382-136	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Pharmaceuticals USA Inc.	LOSARTAN POTASSIUM	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-136-01)
68382-136-06	68382-136	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Pharmaceuticals USA Inc.	LOSARTAN POTASSIUM	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-136-06)
68382-136-10	68382-136	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Pharmaceuticals USA Inc.	LOSARTAN POTASSIUM	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-136-10)
68382-136-16	68382-136	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Pharmaceuticals USA Inc.	LOSARTAN POTASSIUM	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-136-16)
68382-136-24	68382-136	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Pharmaceuticals USA Inc.	LOSARTAN POTASSIUM	50 mg/1	10000 TABLET, FILM COATED in 1 BOTTLE (68382-136-24)