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
16571-114-10	16571-114	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20230822	N/A	ANDA	ANDA217652	Rising Pharma Holdings, Inc.	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-114-10)
16571-114-50	16571-114	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20230822	N/A	ANDA	ANDA217652	Rising Pharma Holdings, Inc.	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16571-114-50)
16571-113-01	16571-113	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20230822	N/A	ANDA	ANDA217652	Rising Pharma Holdings, Inc.	HYDROXYZINE DIHYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-113-01)
16571-113-50	16571-113	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20230822	N/A	ANDA	ANDA217652	Rising Pharma Holdings, Inc.	HYDROXYZINE DIHYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16571-113-50)
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)
60760-990-30	60760-990	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20250319	N/A	ANDA	ANDA217652	ST. MARY'S MEDICAL PARK PHARMACY	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-990-30)