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
71335-0652-8	71335-0652	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20180510	N/A	ANDA	ANDA040907	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	25 mg/1	4 TABLET in 1 BOTTLE (71335-0652-8)
71335-0652-9	71335-0652	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20211227	N/A	ANDA	ANDA040907	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	25 mg/1	6 TABLET in 1 BOTTLE (71335-0652-9)
71335-0652-2	71335-0652	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20180309	N/A	ANDA	ANDA040907	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE (71335-0652-2)
71335-0652-3	71335-0652	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20180411	N/A	ANDA	ANDA040907	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	25 mg/1	7 TABLET in 1 BOTTLE (71335-0652-3)
71335-0652-0	71335-0652	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20211227	N/A	ANDA	ANDA040907	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	25 mg/1	8 TABLET in 1 BOTTLE (71335-0652-0)
68071-4933-7	68071-4933	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20240905	N/A	ANDA	ANDA040907	NuCare Pharmaceuticals,Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	20 TABLET in 1 BOTTLE (68071-4933-7)
68071-4933-9	68071-4933	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20190620	N/A	ANDA	ANDA040907	NuCare Pharmaceuticals,Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE (68071-4933-9)