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
72319-012-03	72319-012	HUMAN PRESCRIPTION DRUG	isosorbide dinitrate and hydralazine hydrochloride	isosorbide dinitrate and hydralazine hydrochloride	TABLET, FILM COATED	ORAL	20240207	N/A	ANDA	ANDA215988	i3 Pharmaceuticals, LLC	HYDRALAZINE HYDROCHLORIDE; ISOSORBIDE DINITRATE	37.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72319-012-03)
72319-012-18	72319-012	HUMAN PRESCRIPTION DRUG	isosorbide dinitrate and hydralazine hydrochloride	isosorbide dinitrate and hydralazine hydrochloride	TABLET, FILM COATED	ORAL	20240207	N/A	ANDA	ANDA215988	i3 Pharmaceuticals, LLC	HYDRALAZINE HYDROCHLORIDE; ISOSORBIDE DINITRATE	37.5 mg/1; 20 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (72319-012-18)
73141-012-03	73141-012	HUMAN PRESCRIPTION DRUG	isosorbide dinitrate and hydralazine hydrochloride	isosorbide dinitrate and hydralazine hydrochloride	TABLET, FILM COATED	ORAL	20240422	N/A	ANDA	ANDA215988	A2A Integrated Pharmaceuticals	HYDRALAZINE HYDROCHLORIDE; ISOSORBIDE DINITRATE	37.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (73141-012-03)
73141-012-18	73141-012	HUMAN PRESCRIPTION DRUG	isosorbide dinitrate and hydralazine hydrochloride	isosorbide dinitrate and hydralazine hydrochloride	TABLET, FILM COATED	ORAL	20240422	N/A	ANDA	ANDA215988	A2A Integrated Pharmaceuticals	HYDRALAZINE HYDROCHLORIDE; ISOSORBIDE DINITRATE	37.5 mg/1; 20 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (73141-012-18)