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=ANDA202491"
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
0093-5004-56 0093-5004 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide TABLET, FILM COATED ORAL 20161114 N/A ANDA ANDA202491 Teva Pharmaceuticals USA, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0093-5004-56)
0093-5006-56 0093-5006 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide TABLET, FILM COATED ORAL 20161114 N/A ANDA ANDA202491 Teva Pharmaceuticals USA, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0093-5006-56)
0093-5005-56 0093-5005 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide TABLET, FILM COATED ORAL 20161114 N/A ANDA ANDA202491 Teva Pharmaceuticals USA, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0093-5005-56)
0093-5002-56 0093-5002 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide TABLET, FILM COATED ORAL 20161114 N/A ANDA ANDA202491 Teva Pharmaceuticals USA, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0093-5002-56)
0093-5003-56 0093-5003 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide TABLET, FILM COATED ORAL 20161114 N/A ANDA ANDA202491 Teva Pharmaceuticals USA, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 12.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0093-5003-56)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase