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
71335-0269-8	71335-0269	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20220209	N/A	ANDA	ANDA202556	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	25 mg/1	4 TABLET in 1 BOTTLE (71335-0269-8)
71335-0269-9	71335-0269	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20220209	N/A	ANDA	ANDA202556	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	25 mg/1	8 TABLET in 1 BOTTLE (71335-0269-9)
71205-090-00	71205-090	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20180801	N/A	ANDA	ANDA202556	Proficient Rx LP	HYDROCHLOROTHIAZIDE	50 mg/1	100 TABLET in 1 BOTTLE (71205-090-00)
71205-090-30	71205-090	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20180801	N/A	ANDA	ANDA202556	Proficient Rx LP	HYDROCHLOROTHIAZIDE	50 mg/1	30 TABLET in 1 BOTTLE (71205-090-30)
71205-090-60	71205-090	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20180801	N/A	ANDA	ANDA202556	Proficient Rx LP	HYDROCHLOROTHIAZIDE	50 mg/1	60 TABLET in 1 BOTTLE (71205-090-60)
71205-090-90	71205-090	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20180801	N/A	ANDA	ANDA202556	Proficient Rx LP	HYDROCHLOROTHIAZIDE	50 mg/1	90 TABLET in 1 BOTTLE (71205-090-90)
71205-090-03	71205-090	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20180801	N/A	ANDA	ANDA202556	Proficient Rx LP	HYDROCHLOROTHIAZIDE	50 mg/1	3 TABLET in 1 BOTTLE (71205-090-03)
71205-090-07	71205-090	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20180801	N/A	ANDA	ANDA202556	Proficient Rx LP	HYDROCHLOROTHIAZIDE	50 mg/1	7 TABLET in 1 BOTTLE (71205-090-07)
71205-090-10	71205-090	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20180801	N/A	ANDA	ANDA202556	Proficient Rx LP	HYDROCHLOROTHIAZIDE	50 mg/1	10 TABLET in 1 BOTTLE (71205-090-10)