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
73043-009-01	73043-009	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20241101	N/A	ANDA	ANDA210416	Devatis, Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	50 mL in 1 BOTTLE (73043-009-01)
73043-009-02	73043-009	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20241101	N/A	ANDA	ANDA210416	Devatis, Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	75 mL in 1 BOTTLE (73043-009-02)
73043-009-03	73043-009	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20241101	N/A	ANDA	ANDA210416	Devatis, Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	100 mL in 1 BOTTLE (73043-009-03)