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
71610-065-45	71610-065	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20180517	N/A	ANDA	ANDA076958	Aphena Pharma Solutions - Tennessee, LLC	LOSARTAN POTASSIUM	25 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71610-065-45)
71610-065-60	71610-065	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20180525	N/A	ANDA	ANDA076958	Aphena Pharma Solutions - Tennessee, LLC	LOSARTAN POTASSIUM	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-065-60)
71610-009-60	71610-009	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20171218	N/A	ANDA	ANDA076958	Aphena Pharma Solutions - Tennessee, LLC	LOSARTAN POTASSIUM	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-009-60)
71610-009-45	71610-009	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20171030	N/A	ANDA	ANDA076958	Aphena Pharma Solutions - Tennessee, LLC	LOSARTAN POTASSIUM	50 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71610-009-45)
71610-009-30	71610-009	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20180612	N/A	ANDA	ANDA076958	Aphena Pharma Solutions - Tennessee, LLC	LOSARTAN POTASSIUM	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71610-009-30)