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
82868-016-90	82868-016	HUMAN PRESCRIPTION DRUG	HYDROCHLOROTHIAZIDE	hydrochlorothiazide	TABLET	ORAL	20231006	N/A	ANDA	ANDA085182	Northwind Health Company, LLC	HYDROCHLOROTHIAZIDE	50 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (82868-016-90)
62135-448-05	62135-448	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20230119	N/A	ANDA	ANDA085182	Chartwell RX, LLC	HYDROCHLOROTHIAZIDE	25 mg/1	500 TABLET in 1 BOTTLE (62135-448-05)
62135-448-90	62135-448	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20230119	N/A	ANDA	ANDA085182	Chartwell RX, LLC	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE (62135-448-90)
70518-4525-0	70518-4525	HUMAN PRESCRIPTION DRUG	HYDROCHLOROTHIAZIDE	hydrochlorothiazide	TABLET	ORAL	20251128	N/A	ANDA	ANDA085182	REMEDYREPACK INC.	HYDROCHLOROTHIAZIDE	50 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-4525-0)