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=ANDA065256"
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
70518-2191-2 70518-2191 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20190719 N/A ANDA ANDA065256 REMEDYREPACK INC. AMOXICILLIN 875 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-2)
70518-2191-3 70518-2191 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20190719 N/A ANDA ANDA065256 REMEDYREPACK INC. AMOXICILLIN 875 mg/1 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-3)
70518-2191-4 70518-2191 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20200708 N/A ANDA ANDA065256 REMEDYREPACK INC. AMOXICILLIN 875 mg/1 14 TABLET, FILM COATED in 1 BLISTER PACK (70518-2191-4)
42708-078-20 42708-078 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20190114 N/A ANDA ANDA065256 QPharma, Inc. AMOXICILLIN 875 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (42708-078-20)
70518-3886-0 70518-3886 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20231005 N/A ANDA ANDA065256 REMEDYREPACK INC. AMOXICILLIN 500 mg/1 100 POUCH in 1 BOX (70518-3886-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3886-1)
76420-003-01 76420-003 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20240821 N/A ANDA ANDA065256 Asclemed USA, Inc. AMOXICILLIN 875 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-003-01)
76420-003-20 76420-003 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20240821 N/A ANDA ANDA065256 Asclemed USA, Inc. AMOXICILLIN 875 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (76420-003-20)
57237-028-01 57237-028 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20051109 N/A ANDA ANDA065256 Rising Pharma Holdings, Inc. AMOXICILLIN 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (57237-028-01)
57237-028-20 57237-028 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20051109 N/A ANDA ANDA065256 Rising Pharma Holdings, Inc. AMOXICILLIN 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (57237-028-20)
68788-7414-2 68788-7414 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20200325 N/A ANDA ANDA065256 Preferred Pharmaceuticals Inc. AMOXICILLIN 875 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68788-7414-2)
68071-5096-2 68071-5096 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20191031 N/A ANDA ANDA065256 NuCare Pharmaceuticals,Inc. AMOXICILLIN 875 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-5096-2)
68071-5096-3 68071-5096 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20191031 N/A ANDA ANDA065256 NuCare Pharmaceuticals,Inc. AMOXICILLIN 875 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-5096-3)
68071-5096-7 68071-5096 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20191031 N/A ANDA ANDA065256 NuCare Pharmaceuticals,Inc. AMOXICILLIN 875 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68071-5096-7)
68071-2911-1 68071-2911 HUMAN PRESCRIPTION DRUG Amoxicillin Amoxicillin TABLET, FILM COATED ORAL 20230110 N/A ANDA ANDA065256 NuCare Pharmaceuticals,Inc. AMOXICILLIN 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68071-2911-1)
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