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
42571-395-77	42571-395	HUMAN PRESCRIPTION DRUG	Amoxicillin and clavulanate potassium	Amoxicillin and clavulanate potassium	FOR SUSPENSION	ORAL	20240401	N/A	ANDA	ANDA217805	Micro Labs Limited	AMOXICILLIN; CLAVULANATE POTASSIUM	600 mg/5mL; 42.9 mg/5mL	200 mL in 1 BOTTLE (42571-395-77)
42571-395-70	42571-395	HUMAN PRESCRIPTION DRUG	Amoxicillin and clavulanate potassium	Amoxicillin and clavulanate potassium	FOR SUSPENSION	ORAL	20240401	N/A	ANDA	ANDA217805	Micro Labs Limited	AMOXICILLIN; CLAVULANATE POTASSIUM	600 mg/5mL; 42.9 mg/5mL	125 mL in 1 BOTTLE (42571-395-70)
42571-395-46	42571-395	HUMAN PRESCRIPTION DRUG	Amoxicillin and clavulanate potassium	Amoxicillin and clavulanate potassium	FOR SUSPENSION	ORAL	20240401	N/A	ANDA	ANDA217805	Micro Labs Limited	AMOXICILLIN; CLAVULANATE POTASSIUM	600 mg/5mL; 42.9 mg/5mL	75 mL in 1 BOTTLE (42571-395-46)