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
68788-8707-6	68788-8707	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240701	N/A	ANDA	ANDA217652	Preferred Pharmaceuticals Inc.	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8707-6)
68788-8707-9	68788-8707	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240701	N/A	ANDA	ANDA217652	Preferred Pharmaceuticals Inc.	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8707-9)
71335-2636-1	71335-2636	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20250602	N/A	ANDA	ANDA217652	Bryant Ranch Prepack	HYDROXYZINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2636-1)
71335-2636-2	71335-2636	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20250602	N/A	ANDA	ANDA217652	Bryant Ranch Prepack	HYDROXYZINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2636-2)
71335-2636-3	71335-2636	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20250602	N/A	ANDA	ANDA217652	Bryant Ranch Prepack	HYDROXYZINE HYDROCHLORIDE	10 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-2636-3)
68788-8872-3	68788-8872	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20250501	N/A	ANDA	ANDA217652	Preferred Pharmaceuticals Inc.	HYDROXYZINE DIHYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8872-3)