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
65862-309-01	65862-309	HUMAN PRESCRIPTION DRUG	Fosinopril Sodium and Hydrochlorothiazide	Fosinopril Sodium and Hydrochlorothiazide	TABLET	ORAL	20090709	N/A	ANDA	ANDA079245	Aurobindo Pharma Limited	FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE	20 mg/1; 12.5 mg/1	100 TABLET in 1 BOTTLE (65862-309-01)
65862-309-30	65862-309	HUMAN PRESCRIPTION DRUG	Fosinopril Sodium and Hydrochlorothiazide	Fosinopril Sodium and Hydrochlorothiazide	TABLET	ORAL	20090709	N/A	ANDA	ANDA079245	Aurobindo Pharma Limited	FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE	20 mg/1; 12.5 mg/1	30 TABLET in 1 BOTTLE (65862-309-30)
65862-309-99	65862-309	HUMAN PRESCRIPTION DRUG	Fosinopril Sodium and Hydrochlorothiazide	Fosinopril Sodium and Hydrochlorothiazide	TABLET	ORAL	20090709	N/A	ANDA	ANDA079245	Aurobindo Pharma Limited	FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE	20 mg/1; 12.5 mg/1	1000 TABLET in 1 BOTTLE (65862-309-99)
65862-308-99	65862-308	HUMAN PRESCRIPTION DRUG	Fosinopril Sodium and Hydrochlorothiazide	Fosinopril Sodium and Hydrochlorothiazide	TABLET	ORAL	20090709	N/A	ANDA	ANDA079245	Aurobindo Pharma Limited	FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE	10 mg/1; 12.5 mg/1	1000 TABLET in 1 BOTTLE (65862-308-99)
65862-308-30	65862-308	HUMAN PRESCRIPTION DRUG	Fosinopril Sodium and Hydrochlorothiazide	Fosinopril Sodium and Hydrochlorothiazide	TABLET	ORAL	20090709	N/A	ANDA	ANDA079245	Aurobindo Pharma Limited	FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE	10 mg/1; 12.5 mg/1	30 TABLET in 1 BOTTLE (65862-308-30)
65862-308-01	65862-308	HUMAN PRESCRIPTION DRUG	Fosinopril Sodium and Hydrochlorothiazide	Fosinopril Sodium and Hydrochlorothiazide	TABLET	ORAL	20090709	N/A	ANDA	ANDA079245	Aurobindo Pharma Limited	FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE	10 mg/1; 12.5 mg/1	100 TABLET in 1 BOTTLE (65862-308-01)