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
62332-029-30	62332-029	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20160523	N/A	ANDA	ANDA090428	Alembic Pharmaceuticals Inc.	LOSARTAN POTASSIUM	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-029-30)
62332-029-31	62332-029	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20160523	N/A	ANDA	ANDA090428	Alembic Pharmaceuticals Inc.	LOSARTAN POTASSIUM	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62332-029-31)
62332-029-90	62332-029	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20160523	N/A	ANDA	ANDA090428	Alembic Pharmaceuticals Inc.	LOSARTAN POTASSIUM	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-029-90)
62332-029-91	62332-029	HUMAN PRESCRIPTION DRUG	Losartan Potassium	Losartan Potassium	TABLET, FILM COATED	ORAL	20160523	N/A	ANDA	ANDA090428	Alembic Pharmaceuticals Inc.	LOSARTAN POTASSIUM	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62332-029-91)