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"
符合检索条件的记录共 26 条，共 2 页，当前第 1 页 ，可点击列名称排序
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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
0713-0876-30 0713-0876 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20220901 N/A NDA NDA200175 Cosette Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0713-0876-30)
0713-0875-30 0713-0875 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20220901 N/A NDA NDA200175 Cosette Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0713-0875-30)
0713-0874-30 0713-0874 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20220901 N/A NDA NDA200175 Cosette Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0713-0874-30)
0713-0877-30 0713-0877 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20220901 N/A NDA NDA200175 Cosette Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 12.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0713-0877-30)
57664-799-83 57664-799 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide olmesartan medoxomil, amlodipine besylate and hydrochlorothiazide TABLET, FILM COATED ORAL 20161026 20240630 NDA AUTHORIZED GENERIC NDA200175 Sun Pharmaceutical Industries, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-799-83)
57664-799-99 57664-799 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide olmesartan medoxomil, amlodipine besylate and hydrochlorothiazide TABLET, FILM COATED ORAL 20161026 20240630 NDA AUTHORIZED GENERIC NDA200175 Sun Pharmaceutical Industries, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-799-99)
57664-800-83 57664-800 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide olmesartan medoxomil, amlodipine besylate and hydrochlorothiazide TABLET, FILM COATED ORAL 20161026 20240531 NDA AUTHORIZED GENERIC NDA200175 Sun Pharmaceutical Industries, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-800-83)
57664-800-99 57664-800 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide olmesartan medoxomil, amlodipine besylate and hydrochlorothiazide TABLET, FILM COATED ORAL 20161026 20240531 NDA AUTHORIZED GENERIC NDA200175 Sun Pharmaceutical Industries, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 25 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-800-99)
0713-0878-30 0713-0878 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20220901 N/A NDA NDA200175 Cosette Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0713-0878-30)
57664-796-83 57664-796 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide olmesartan medoxomil, amlodipine besylate and hydrochlorothiazide TABLET, FILM COATED ORAL 20161026 20240731 NDA AUTHORIZED GENERIC NDA200175 Sun Pharmaceutical Industries, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-796-83)
57664-796-99 57664-796 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide olmesartan medoxomil, amlodipine besylate and hydrochlorothiazide TABLET, FILM COATED ORAL 20161026 20240731 NDA AUTHORIZED GENERIC NDA200175 Sun Pharmaceutical Industries, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-796-99)
65597-114-07 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 BOTTLE (65597-114-07)
65597-114-90 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 90 TABLET, FILM COATED in 1 BOTTLE (65597-114-90)
65597-116-07 65597-116 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20100731 20240630 NDA NDA200175 Daiichi Sankyo, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (65597-116-07)
65597-116-10 65597-116 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20100731 20240630 NDA NDA200175 Daiichi Sankyo, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 10 BLISTER PACK in 1 BOX (65597-116-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65597-116-30 65597-116 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20100731 20240630 NDA NDA200175 Daiichi Sankyo, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65597-116-30)
65597-116-70 65597-116 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20100731 20240630 NDA NDA200175 Daiichi Sankyo, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 7 TABLET, FILM COATED in 1 BLISTER PACK (65597-116-70)
65597-116-90 65597-116 HUMAN PRESCRIPTION DRUG Tribenzor olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide TABLET, FILM COATED ORAL 20100731 20240630 NDA NDA200175 Daiichi Sankyo, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65597-116-90)
65597-117-07 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 BOTTLE (65597-117-07)
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
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