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
65841-730-16	65841-730	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Lifesciences Limited	LOSARTAN POTASSIUM	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65841-730-16)
65841-730-24	65841-730	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Lifesciences Limited	LOSARTAN POTASSIUM	50 mg/1	10000 TABLET, FILM COATED in 1 BOTTLE (65841-730-24)
65841-731-01	65841-731	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Lifesciences Limited	LOSARTAN POTASSIUM	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-731-01)
65841-731-06	65841-731	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Lifesciences Limited	LOSARTAN POTASSIUM	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65841-731-06)
65841-731-10	65841-731	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Lifesciences Limited	LOSARTAN POTASSIUM	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-731-10)
65841-731-16	65841-731	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Lifesciences Limited	LOSARTAN POTASSIUM	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65841-731-16)
65841-731-77	65841-731	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Lifesciences Limited	LOSARTAN POTASSIUM	100 mg/1	10 BLISTER PACK in 1 CARTON (65841-731-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65841-731-30)
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)
82009-043-10	82009-043	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20220920	N/A	ANDA	ANDA078243	Quallent Pharmaceuticals Health LLC	LOSARTAN POTASSIUM	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (82009-043-10)
82009-044-10	82009-044	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20220920	N/A	ANDA	ANDA078243	Quallent Pharmaceuticals Health LLC	LOSARTAN POTASSIUM	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (82009-044-10)
65841-729-06	65841-729	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Lifesciences Limited	LOSARTAN POTASSIUM	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65841-729-06)
65841-729-10	65841-729	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Lifesciences Limited	LOSARTAN POTASSIUM	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-729-10)
65841-729-16	65841-729	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20101004	N/A	ANDA	ANDA078243	Zydus Lifesciences Limited	LOSARTAN POTASSIUM	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65841-729-16)