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
71335-1976-7	71335-1976	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20211221	N/A	ANDA	ANDA040907	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	50 mg/1	7 TABLET in 1 BOTTLE (71335-1976-7)
71335-1976-8	71335-1976	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20211221	N/A	ANDA	ANDA040907	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	50 mg/1	14 TABLET in 1 BOTTLE (71335-1976-8)
71335-1976-9	71335-1976	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20211221	N/A	ANDA	ANDA040907	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	50 mg/1	120 TABLET in 1 BOTTLE (71335-1976-9)
82804-031-30	82804-031	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20231024	N/A	ANDA	ANDA040907	Proficient Rx LP	HYDROCHLOROTHIAZIDE	50 mg/1	30 TABLET in 1 BOTTLE (82804-031-30)
82804-031-60	82804-031	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20231024	N/A	ANDA	ANDA040907	Proficient Rx LP	HYDROCHLOROTHIAZIDE	50 mg/1	60 TABLET in 1 BOTTLE (82804-031-60)
82804-031-90	82804-031	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20231024	N/A	ANDA	ANDA040907	Proficient Rx LP	HYDROCHLOROTHIAZIDE	50 mg/1	90 TABLET in 1 BOTTLE (82804-031-90)
50090-5057-0	50090-5057	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20200522	N/A	ANDA	ANDA040907	A-S Medication Solutions	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE (50090-5057-0)
51655-422-26	51655-422	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20221229	N/A	ANDA	ANDA040907	Northwind Pharmaceuticals, LLC	HYDROCHLOROTHIAZIDE	50 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-422-26)
51655-422-52	51655-422	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20230606	N/A	ANDA	ANDA040907	Northwind Pharmaceuticals, LLC	HYDROCHLOROTHIAZIDE	50 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-422-52)
55700-006-30	55700-006	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20090702	N/A	ANDA	ANDA040907	Lake Erie Medical DBA Quality Care Products LLC	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE (55700-006-30)
55700-006-90	55700-006	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20090702	N/A	ANDA	ANDA040907	Lake Erie Medical DBA Quality Care Products LLC	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE (55700-006-90)
68071-3238-1	68071-3238	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20170609	N/A	ANDA	ANDA040907	NuCare Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	100 TABLET in 1 BOTTLE (68071-3238-1)
42708-079-30	42708-079	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20190211	N/A	ANDA	ANDA040907	QPharma Inc	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE (42708-079-30)
53002-4973-0	53002-4973	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20230831	N/A	ANDA	ANDA040907	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	100 TABLET in 1 BOTTLE (53002-4973-0)
53002-4973-3	53002-4973	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20230831	N/A	ANDA	ANDA040907	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE (53002-4973-3)
53002-4973-6	53002-4973	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20230831	N/A	ANDA	ANDA040907	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	60 TABLET in 1 BOTTLE (53002-4973-6)
72789-303-01	72789-303	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20220302	N/A	ANDA	ANDA040907	PD-Rx Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	50 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (72789-303-01)