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
63629-5696-5	63629-5696	HUMAN PRESCRIPTION DRUG	HYDRALAZINE HYDROCHLORIDE	hydralazine hydrochloride	TABLET, FILM COATED	ORAL	20260403	20260831	ANDA	ANDA086242	Bryant Ranch Prepack	HYDRALAZINE HYDROCHLORIDE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (63629-5696-5)
63629-5696-2	63629-5696	HUMAN PRESCRIPTION DRUG	HYDRALAZINE HYDROCHLORIDE	hydralazine hydrochloride	TABLET, FILM COATED	ORAL	20160624	20260831	ANDA	ANDA086242	Bryant Ranch Prepack	HYDRALAZINE HYDROCHLORIDE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-5696-2)
63629-5696-3	63629-5696	HUMAN PRESCRIPTION DRUG	HYDRALAZINE HYDROCHLORIDE	hydralazine hydrochloride	TABLET, FILM COATED	ORAL	20150715	20260831	ANDA	ANDA086242	Bryant Ranch Prepack	HYDRALAZINE HYDROCHLORIDE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-5696-3)
63629-5696-4	63629-5696	HUMAN PRESCRIPTION DRUG	HYDRALAZINE HYDROCHLORIDE	hydralazine hydrochloride	TABLET, FILM COATED	ORAL	20240402	20260831	ANDA	ANDA086242	Bryant Ranch Prepack	HYDRALAZINE HYDROCHLORIDE	25 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (63629-5696-4)