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）

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
59651-025-75	59651-025	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20190419	N/A	ANDA	ANDA209371	Aurobindo Pharma Limited	AMOXICILLIN; CLAVULANATE POTASSIUM	125 mg/5mL; 31.25 mg/5mL	75 mL in 1 BOTTLE (59651-025-75)
59651-025-55	59651-025	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20190419	N/A	ANDA	ANDA209371	Aurobindo Pharma Limited	AMOXICILLIN; CLAVULANATE POTASSIUM	125 mg/5mL; 31.25 mg/5mL	150 mL in 1 BOTTLE (59651-025-55)
59651-025-01	59651-025	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20190419	N/A	ANDA	ANDA209371	Aurobindo Pharma Limited	AMOXICILLIN; CLAVULANATE POTASSIUM	125 mg/5mL; 31.25 mg/5mL	100 mL in 1 BOTTLE (59651-025-01)
59651-026-01	59651-026	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20190419	N/A	ANDA	ANDA209371	Aurobindo Pharma Limited	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/5mL; 62.5 mg/5mL	100 mL in 1 BOTTLE (59651-026-01)
59651-026-55	59651-026	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20190419	N/A	ANDA	ANDA209371	Aurobindo Pharma Limited	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/5mL; 62.5 mg/5mL	150 mL in 1 BOTTLE (59651-026-55)
59651-026-75	59651-026	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20190419	N/A	ANDA	ANDA209371	Aurobindo Pharma Limited	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/5mL; 62.5 mg/5mL	75 mL in 1 BOTTLE (59651-026-75)