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
42806-161-05	42806-161	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20150331	N/A	ANDA	ANDA040604	Epic Pharma, LLC	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42806-161-05)
42806-161-10	42806-161	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20150331	N/A	ANDA	ANDA040604	Epic Pharma, LLC	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42806-161-10)
42806-161-01	42806-161	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20150331	N/A	ANDA	ANDA040604	Epic Pharma, LLC	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42806-161-01)
68071-5133-6	68071-5133	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20191213	N/A	ANDA	ANDA040604	NuCare Pharmaceuticals,Inc.	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-5133-6)
68071-5133-3	68071-5133	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20241015	N/A	ANDA	ANDA040604	NuCare Pharmaceuticals,Inc.	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-5133-3)
24658-783-10	24658-783	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20210721	N/A	ANDA	ANDA040604	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (24658-783-10)