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
72789-296-90	72789-296	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20221228	N/A	ANDA	ANDA087059	PD-Rx Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (72789-296-90)
72789-296-60	72789-296	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20230727	N/A	ANDA	ANDA087059	PD-Rx Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (72789-296-60)
72789-296-30	72789-296	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20221230	N/A	ANDA	ANDA087059	PD-Rx Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-296-30)
69584-361-10	69584-361	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20200925	N/A	ANDA	ANDA087059	Oxford Pharmaceuticals, LLC	HYDROCHLOROTHIAZIDE	25 mg/1	100 TABLET in 1 BOTTLE (69584-361-10)
69584-361-90	69584-361	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20200925	N/A	ANDA	ANDA087059	Oxford Pharmaceuticals, LLC	HYDROCHLOROTHIAZIDE	25 mg/1	1000 TABLET in 1 BOTTLE (69584-361-90)
69584-361-95	69584-361	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20200925	N/A	ANDA	ANDA087059	Oxford Pharmaceuticals, LLC	HYDROCHLOROTHIAZIDE	25 mg/1	5000 TABLET in 1 BOTTLE (69584-361-95)
51655-088-26	51655-088	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20240325	N/A	ANDA	ANDA087059	Northwind Pharmaceuticals, LLC	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-088-26)
51655-088-52	51655-088	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20230306	N/A	ANDA	ANDA087059	Northwind Pharmaceuticals, LLC	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-088-52)
72789-381-90	72789-381	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20240220	N/A	ANDA	ANDA087059	PD-Rx Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (72789-381-90)
50090-6157-1	50090-6157	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20221007	N/A	ANDA	ANDA087059	A-S Medication Solutions	HYDROCHLOROTHIAZIDE	25 mg/1	100 TABLET in 1 BOTTLE (50090-6157-1)
50090-6160-0	50090-6160	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20221007	N/A	ANDA	ANDA087059	A-S Medication Solutions	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE (50090-6160-0)
50090-6157-8	50090-6157	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20221007	N/A	ANDA	ANDA087059	A-S Medication Solutions	HYDROCHLOROTHIAZIDE	25 mg/1	200 TABLET in 1 BOTTLE (50090-6157-8)
50090-6157-0	50090-6157	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20221007	N/A	ANDA	ANDA087059	A-S Medication Solutions	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE (50090-6157-0)
50090-6158-0	50090-6158	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20221007	N/A	ANDA	ANDA087059	A-S Medication Solutions	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE (50090-6158-0)
70518-4113-0	70518-4113	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20240626	N/A	ANDA	ANDA087059	REMEDYREPACK INC.	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BLISTER PACK (70518-4113-0)