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
16714-295-01	16714-295	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20120120	N/A	ANDA	ANDA091569	NorthStar Rx LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/1; 125 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16714-295-01)
65862-502-05	65862-502	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20120120	N/A	ANDA	ANDA091569	Aurobindo Pharma Limited	AMOXICILLIN; CLAVULANATE POTASSIUM	500 mg/1; 125 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-502-05)
65862-502-20	65862-502	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20120120	N/A	ANDA	ANDA091569	Aurobindo Pharma Limited	AMOXICILLIN; CLAVULANATE POTASSIUM	500 mg/1; 125 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (65862-502-20)
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)
50090-6997-0	50090-6997	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20231227	N/A	ANDA	ANDA091569	A-S Medication Solutions	AMOXICILLIN; CLAVULANATE POTASSIUM	500 mg/1; 125 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (50090-6997-0)