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
45865-927-01	45865-927	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20181212	N/A	ANDA	ANDA065098	medsource pharmaceuticals	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	75 mL in 1 BOTTLE (45865-927-01)
66685-1011-2	66685-1011	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20040813	N/A	ANDA	ANDA065098	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	200 mg/5mL; 28.5 mg/5mL	100 mL in 1 BOTTLE (66685-1011-2)
66685-1012-1	66685-1012	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20040813	N/A	ANDA	ANDA065098	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	75 mL in 1 BOTTLE (66685-1012-1)
66685-1012-2	66685-1012	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20040813	N/A	ANDA	ANDA065098	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	100 mL in 1 BOTTLE (66685-1012-2)
66685-1011-1	66685-1011	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20040813	N/A	ANDA	ANDA065098	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	200 mg/5mL; 28.5 mg/5mL	75 mL in 1 BOTTLE (66685-1011-1)
66685-1011-0	66685-1011	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20040813	N/A	ANDA	ANDA065098	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	200 mg/5mL; 28.5 mg/5mL	50 mL in 1 BOTTLE (66685-1011-0)
50090-6381-0	50090-6381	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20230227	N/A	ANDA	ANDA065098	A-S Medication Solutions	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	50 mL in 1 BOTTLE (50090-6381-0)
66685-1012-0	66685-1012	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20040813	N/A	ANDA	ANDA065098	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	50 mL in 1 BOTTLE (66685-1012-0)
53002-0050-1	53002-0050	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20190101	N/A	ANDA	ANDA065098	RPK Pharmaceuticals, Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	200 mg/5mL; 28.5 mg/5mL	50 mL in 1 BOTTLE (53002-0050-1)
63187-542-00	63187-542	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	POWDER, FOR SUSPENSION	ORAL	20181201	N/A	ANDA	ANDA065098	Proficient Rx LP	AMOXICILLIN; CLAVULANATE POTASSIUM	200 mg/5mL; 28.5 mg/5mL	100 mL in 1 BOTTLE (63187-542-00)