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
57237-032-01	57237-032	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20061228	N/A	ANDA	ANDA065334	Rising Pharma Holdings, Inc.	AMOXICILLIN	200 mg/5mL	100 mL in 1 BOTTLE (57237-032-01)
63187-262-50	63187-262	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20240111	N/A	ANDA	ANDA065334	Proficient Rx LP	AMOXICILLIN	400 mg/5mL	50 mL in 1 BOTTLE (63187-262-50)
63187-262-00	63187-262	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20150202	N/A	ANDA	ANDA065334	Proficient Rx LP	AMOXICILLIN	400 mg/5mL	100 mL in 1 BOTTLE (63187-262-00)
63187-335-00	63187-335	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20190101	N/A	ANDA	ANDA065334	Proficient Rx LP	AMOXICILLIN	400 mg/5mL	100 mL in 1 BOTTLE (63187-335-00)
50090-6680-0	50090-6680	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20230908	N/A	ANDA	ANDA065334	A-S Medication Solutions	AMOXICILLIN	400 mg/5mL	50 mL in 1 BOTTLE (50090-6680-0)