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=ANDA091569"
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
68071-5065-3 68071-5065 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20190920 N/A ANDA ANDA091569 NuCare Pharmaceuticals,Inc. AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (68071-5065-3)
68071-5065-4 68071-5065 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20190920 N/A ANDA ANDA091569 NuCare Pharmaceuticals,Inc. AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (68071-5065-4)
60687-781-94 60687-781 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20240726 N/A ANDA ANDA091569 American Health Packaging AMOXICILLIN; CLAVULANATE POTASSIUM 250 mg/1; 125 mg/1 20 BLISTER PACK in 1 CARTON (60687-781-94) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-781-11)
85766-079-20 85766-079 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20251015 N/A ANDA ANDA091569 Sportpharm, Inc. dba Sportpharm AMOXICILLIN; CLAVULANATE POTASSIUM 500 mg/1; 125 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (85766-079-20)
85766-080-30 85766-080 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20251015 N/A ANDA ANDA091569 Sportpharm, Inc. dba Sportpharm AMOXICILLIN; CLAVULANATE POTASSIUM 250 mg/1; 125 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (85766-080-30)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase