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)
检索条件:" 注册申请号=NDA200175"
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
65597-114-30 65597-114 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20100731 20240831 NDA NDA200175 Daiichi Sankyo, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65597-114-30)
65597-114-70 65597-114 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20100731 20240831 NDA NDA200175 Daiichi Sankyo, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 20 mg/1 7 TABLET, FILM COATED in 1 BLISTER PACK (65597-114-70)
65597-117-10 65597-117 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20100731 20240531 NDA NDA200175 Daiichi Sankyo, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 12.5 mg/1; 40 mg/1 10 BLISTER PACK in 1 BOX (65597-117-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65597-117-30 65597-117 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20100731 20240531 NDA NDA200175 Daiichi Sankyo, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 12.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65597-117-30)
65597-117-70 65597-117 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20100731 20240531 NDA NDA200175 Daiichi Sankyo, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 12.5 mg/1; 40 mg/1 7 TABLET, FILM COATED in 1 BLISTER PACK (65597-117-70)
65597-117-90 65597-117 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20100731 20240531 NDA NDA200175 Daiichi Sankyo, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 12.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65597-117-90)
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