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
70518-4049-0	70518-4049	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240411	N/A	ANDA	ANDA217652	REMEDYREPACK INC.	HYDROXYZINE DIHYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4049-0)
71335-2410-1	71335-2410	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240610	N/A	ANDA	ANDA217652	Bryant Ranch Prepack	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2410-1)
71335-2410-2	71335-2410	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240610	N/A	ANDA	ANDA217652	Bryant Ranch Prepack	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-2410-2)
71335-2410-3	71335-2410	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240610	N/A	ANDA	ANDA217652	Bryant Ranch Prepack	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2410-3)
71335-2410-4	71335-2410	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240610	N/A	ANDA	ANDA217652	Bryant Ranch Prepack	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2410-4)
71335-2410-5	71335-2410	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240610	N/A	ANDA	ANDA217652	Bryant Ranch Prepack	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2410-5)
16571-114-01	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	100 TABLET, FILM COATED in 1 BOTTLE (16571-114-01)
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)
69844-072-01	69844-072	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20230822	N/A	ANDA	ANDA217652	Graviti Pharmaceuticals Private Limited	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69844-072-01)
69844-072-02	69844-072	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20230822	N/A	ANDA	ANDA217652	Graviti Pharmaceuticals Private Limited	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69844-072-02)
69844-072-03	69844-072	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20230822	N/A	ANDA	ANDA217652	Graviti Pharmaceuticals Private Limited	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69844-072-03)
68788-8707-3	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	30 TABLET, FILM COATED in 1 BOTTLE (68788-8707-3)
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)
50090-7330-0	50090-7330	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20241015	N/A	ANDA	ANDA217652	A-S Medication Solutions	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-7330-0)
50090-7330-1	50090-7330	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20241015	N/A	ANDA	ANDA217652	A-S Medication Solutions	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-7330-1)
50090-7330-4	50090-7330	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20241015	N/A	ANDA	ANDA217652	A-S Medication Solutions	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-7330-4)
69844-073-01	69844-073	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20230822	N/A	ANDA	ANDA217652	Graviti Pharmaceuticals Private Limited	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69844-073-01)
69844-073-02	69844-073	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20230822	N/A	ANDA	ANDA217652	Graviti Pharmaceuticals Private Limited	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69844-073-02)