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
59651-499-01	59651-499	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA087871	Aurobindo Pharma Limited	HYDROXYZINE DIHYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-499-01)
59651-499-05	59651-499	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA087871	Aurobindo Pharma Limited	HYDROXYZINE DIHYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (59651-499-05)
59651-499-78	59651-499	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA087871	Aurobindo Pharma Limited	HYDROXYZINE DIHYDROCHLORIDE	10 mg/1	10 BLISTER PACK in 1 CARTON (59651-499-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK
59651-499-99	59651-499	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA087871	Aurobindo Pharma Limited	HYDROXYZINE DIHYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (59651-499-99)
59651-500-01	59651-500	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA087871	Aurobindo Pharma Limited	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-500-01)
59651-500-05	59651-500	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA087871	Aurobindo Pharma Limited	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (59651-500-05)
59651-500-99	59651-500	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA087871	Aurobindo Pharma Limited	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (59651-500-99)
59651-501-01	59651-501	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA087871	Aurobindo Pharma Limited	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-501-01)
59651-501-05	59651-501	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA087871	Aurobindo Pharma Limited	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (59651-501-05)
59651-501-99	59651-501	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA087871	Aurobindo Pharma Limited	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (59651-501-99)
70518-4131-0	70518-4131	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20240701	N/A	ANDA	ANDA087871	REMEDYREPACK INC.	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4131-0)
80425-0376-1	80425-0376	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20240313	N/A	ANDA	ANDA087871	Advanced Rx Pharmacy of Tennessee, LLC	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0376-1)
80425-0376-2	80425-0376	HUMAN PRESCRIPTION DRUG	Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	TABLET, FILM COATED	ORAL	20240425	N/A	ANDA	ANDA087871	Advanced Rx Pharmacy of Tennessee, LLC	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0376-2)