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
13668-397-05	13668-397	HUMAN PRESCRIPTION DRUG	Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 20/5/12.5 mg	Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Tablet 20/5/12.5 mg	TABLET	ORAL	20161026	20260131	ANDA	ANDA203580	Torrent Pharmaceuticals Limited	AMLODIPINE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 12.5 mg/1; 20 mg/1	500 TABLET in 1 BOTTLE (13668-397-05)
13668-397-30	13668-397	HUMAN PRESCRIPTION DRUG	Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 20/5/12.5 mg	Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Tablet 20/5/12.5 mg	TABLET	ORAL	20161026	20260131	ANDA	ANDA203580	Torrent Pharmaceuticals Limited	AMLODIPINE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 12.5 mg/1; 20 mg/1	30 TABLET in 1 BOTTLE (13668-397-30)
13668-397-90	13668-397	HUMAN PRESCRIPTION DRUG	Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 20/5/12.5 mg	Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Tablet 20/5/12.5 mg	TABLET	ORAL	20161026	20260131	ANDA	ANDA203580	Torrent Pharmaceuticals Limited	AMLODIPINE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 12.5 mg/1; 20 mg/1	90 TABLET in 1 BOTTLE (13668-397-90)