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
73043-010-01	73043-010	HUMAN PRESCRIPTION DRUG	amoxicillin and clavulanate potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20240815	N/A	ANDA	ANDA210374	Devatis, Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/5mL; 62.5 mg/5mL	75 mL in 1 BOTTLE (73043-010-01)
73043-010-02	73043-010	HUMAN PRESCRIPTION DRUG	amoxicillin and clavulanate potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20240901	N/A	ANDA	ANDA210374	Devatis, Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/5mL; 62.5 mg/5mL	100 mL in 1 BOTTLE (73043-010-02)
73043-010-03	73043-010	HUMAN PRESCRIPTION DRUG	amoxicillin and clavulanate potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20240705	N/A	ANDA	ANDA210374	Devatis, Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/5mL; 62.5 mg/5mL	150 mL in 1 BOTTLE (73043-010-03)