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
71335-2185-3	71335-2185	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA040604	Bryant Ranch Prepack	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2185-3)
71335-2185-4	71335-2185	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20221129	N/A	ANDA	ANDA040604	Bryant Ranch Prepack	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2185-4)
71335-2185-5	71335-2185	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA040604	Bryant Ranch Prepack	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2185-5)
42806-160-01	42806-160	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20150331	N/A	ANDA	ANDA040604	Epic Pharma, LLC	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42806-160-01)
42806-160-05	42806-160	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20150331	N/A	ANDA	ANDA040604	Epic Pharma, LLC	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42806-160-05)
42806-160-10	42806-160	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20150331	N/A	ANDA	ANDA040604	Epic Pharma, LLC	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42806-160-10)
55154-7994-0	55154-7994	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20150331	20260831	ANDA	ANDA040604	Cardinal Health 107, LLC	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	10 BLISTER PACK in 1 BAG (55154-7994-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK