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=ANDA207771"
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
68382-930-01 68382-930 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 10 mg/1; 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-930-01)
68382-930-05 68382-930 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 10 mg/1; 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-930-05)
68382-930-06 68382-930 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 10 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-930-06)
68382-930-10 68382-930 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 10 mg/1; 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-930-10)
68382-930-16 68382-930 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 10 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-930-16)
68382-930-77 68382-930 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 10 mg/1; 40 mg/1 10 BLISTER PACK in 1 CARTON (68382-930-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-930-30)
68382-929-01 68382-929 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-929-01)
68382-929-05 68382-929 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-929-05)
68382-929-06 68382-929 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-929-06)
68382-929-10 68382-929 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-929-10)
68382-929-16 68382-929 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-929-16)
68382-929-77 68382-929 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 40 mg/1 10 BLISTER PACK in 1 CARTON (68382-929-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-929-30)
68382-927-01 68382-927 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-927-01)
68382-927-05 68382-927 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-927-05)
68382-927-06 68382-927 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-927-06)
68382-927-10 68382-927 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-927-10)
68382-927-16 68382-927 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Pharmaceuticals USA Inc. AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-927-16)
70771-1186-0 70771-1186 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Lifesciences Limited AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1186-0)
70771-1186-1 70771-1186 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Lifesciences Limited AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1186-1)
70771-1186-3 70771-1186 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan medoxomil Amlodipine and olmesartan medoxomil TABLET, FILM COATED ORAL 20180104 N/A ANDA ANDA207771 Zydus Lifesciences Limited AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1186-3)
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