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
65862-837-05	65862-837	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 25 mg/1; 160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-837-05)
65862-837-30	65862-837	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 25 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-837-30)
65862-837-90	65862-837	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 25 mg/1; 160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-837-90)
65862-834-05	65862-834	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	5 mg/1; 12.5 mg/1; 160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-834-05)
65862-834-30	65862-834	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	5 mg/1; 12.5 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-834-30)
65862-834-90	65862-834	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	5 mg/1; 12.5 mg/1; 160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-834-90)
65862-838-05	65862-838	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 25 mg/1; 320 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-838-05)
65862-838-30	65862-838	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 25 mg/1; 320 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-838-30)
65862-838-90	65862-838	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 25 mg/1; 320 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-838-90)
65862-835-05	65862-835	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	5 mg/1; 25 mg/1; 160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-835-05)
65862-835-30	65862-835	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	5 mg/1; 25 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-835-30)
65862-835-90	65862-835	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	5 mg/1; 25 mg/1; 160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-835-90)
65862-836-05	65862-836	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 12.5 mg/1; 160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-836-05)
65862-836-30	65862-836	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 12.5 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-836-30)
65862-836-90	65862-836	HUMAN PRESCRIPTION DRUG	Amlodipine, Valsartan and Hydrochlorothiazide	Amlodipine, Valsartan and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20171219	N/A	ANDA	ANDA206180	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 12.5 mg/1; 160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-836-90)