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
51655-305-83	51655-305	HUMAN PRESCRIPTION DRUG	HYDRALAZINE HYDROCHLORIDE	hydralazine hydrochloride	TABLET, FILM COATED	ORAL	20200528	20260831	ANDA	ANDA086242	Northwind Health Company, LLC	HYDRALAZINE HYDROCHLORIDE	25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-305-83)
51655-916-26	51655-916	HUMAN PRESCRIPTION DRUG	HYDRALAZINE HYDROCHLORIDE	hydralazine hydrochloride	TABLET, FILM COATED	ORAL	20200526	20260831	ANDA	ANDA086242	Northwind Health Company, LLC	HYDRALAZINE HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-916-26)
51655-916-52	51655-916	HUMAN PRESCRIPTION DRUG	HYDRALAZINE HYDROCHLORIDE	hydralazine hydrochloride	TABLET, FILM COATED	ORAL	20230712	20260831	ANDA	ANDA086242	Northwind Health Company, LLC	HYDRALAZINE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-916-52)