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=ANDA065063"
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
70518-3624-2 70518-3624 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20250212 N/A ANDA ANDA065063 REMEDYREPACK INC. AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3624-2)
70518-3624-3 70518-3624 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20250313 N/A ANDA ANDA065063 REMEDYREPACK INC. AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3624-3)
72162-2211-2 72162-2211 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20020314 N/A ANDA ANDA065063 Bryant Ranch Prepack AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (72162-2211-2)
16714-014-02 16714-014 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20230307 20260228 ANDA ANDA065063 Northstar RxLLC AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-014-02)
68071-2982-2 68071-2982 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20230419 N/A ANDA ANDA065063 NuCare Pharmaceuticals,Inc. AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-2982-2)
68071-3842-2 68071-3842 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20250507 N/A ANDA ANDA065063 NuCare Pharmaceuticals, Inc. AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-3842-2)
68071-3866-3 68071-3866 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20250613 N/A ANDA ANDA065063 NuCare Pharmaceuticals, Inc. AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3866-3)
68071-3822-3 68071-3822 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20250402 N/A ANDA ANDA065063 NuCare Pharmaceuticals, Inc. AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (68071-3822-3)
0781-1852-13 0781-1852 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20020314 N/A ANDA ANDA065063 Sandoz Inc AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0781-1852-13)
0781-1852-20 0781-1852 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20020314 N/A ANDA ANDA065063 Sandoz Inc AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (0781-1852-20)
0781-1852-01 0781-1852 HUMAN PRESCRIPTION DRUG Amoxicillin and Clavulanate Potassium Amoxicillin and Clavulanate Potassium TABLET, FILM COATED ORAL 20220920 N/A ANDA ANDA065063 Sandoz Inc AMOXICILLIN; CLAVULANATE POTASSIUM 875 mg/1; 125 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0781-1852-01)
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