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
51655-831-52	51655-831	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20230306	N/A	ANDA	ANDA083177	Northwind Pharmaceuticals, LLC	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-831-52)
50090-6014-0	50090-6014	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20220623	N/A	ANDA	ANDA083177	A-S Medication Solutions	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE (50090-6014-0)
53002-4972-0	53002-4972	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20220901	N/A	ANDA	ANDA083177	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	100 TABLET in 1 BOTTLE (53002-4972-0)
53002-4972-1	53002-4972	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20220901	N/A	ANDA	ANDA083177	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	10 TABLET in 1 BOTTLE (53002-4972-1)
53002-4972-3	53002-4972	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20220901	N/A	ANDA	ANDA083177	RPK Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE (53002-4972-3)