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
70518-4359-2	70518-4359	HUMAN PRESCRIPTION DRUG	HYDROCHLOROTHIAZIDE	hydrochlorothiazide	TABLET	ORAL	20250724	N/A	ANDA	ANDA085182	REMEDYREPACK INC.	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-4359-2)
70518-4359-0	70518-4359	HUMAN PRESCRIPTION DRUG	HYDROCHLOROTHIAZIDE	hydrochlorothiazide	TABLET	ORAL	20250616	N/A	ANDA	ANDA085182	REMEDYREPACK INC.	HYDROCHLOROTHIAZIDE	25 mg/1	15 TABLET in 1 BOTTLE, PLASTIC (70518-4359-0)
70518-4359-1	70518-4359	HUMAN PRESCRIPTION DRUG	HYDROCHLOROTHIAZIDE	hydrochlorothiazide	TABLET	ORAL	20250707	N/A	ANDA	ANDA085182	REMEDYREPACK INC.	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BLISTER PACK (70518-4359-1)
68071-5211-2	68071-5211	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20200317	N/A	ANDA	ANDA085182	NuCare Pharmaceuticals,Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	120 TABLET in 1 BOTTLE (68071-5211-2)
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)
51655-272-26	51655-272	HUMAN PRESCRIPTION DRUG	HYDROCHLOROTHIAZIDE	hydrochlorothiazide	TABLET	ORAL	20200504	N/A	ANDA	ANDA085182	Northwind Pharmaceuticals, LLC	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-272-26)
51655-272-52	51655-272	HUMAN PRESCRIPTION DRUG	HYDROCHLOROTHIAZIDE	hydrochlorothiazide	TABLET	ORAL	20230207	N/A	ANDA	ANDA085182	Northwind Pharmaceuticals, LLC	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-272-52)