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
50090-0820-0	50090-0820	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA091569	A-S Medication Solutions	AMOXICILLIN; CLAVULANATE POTASSIUM	500 mg/1; 125 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-0820-0)
50090-0820-1	50090-0820	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA091569	A-S Medication Solutions	AMOXICILLIN; CLAVULANATE POTASSIUM	500 mg/1; 125 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (50090-0820-1)
50090-0820-2	50090-0820	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA091569	A-S Medication Solutions	AMOXICILLIN; CLAVULANATE POTASSIUM	500 mg/1; 125 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-0820-2)
50090-0820-3	50090-0820	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA091569	A-S Medication Solutions	AMOXICILLIN; CLAVULANATE POTASSIUM	500 mg/1; 125 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (50090-0820-3)