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
68071-5208-1	68071-5208	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20200316	N/A	ANDA	ANDA065089	NuCare Pharmaceuticals,Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	100 mL in 1 BOTTLE (68071-5208-1)
63187-770-00	63187-770	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20161101	N/A	ANDA	ANDA065089	Proficient Rx LP	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	100 mL in 1 BOTTLE (63187-770-00)
53002-0100-2	53002-0100	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20190101	N/A	ANDA	ANDA065089	RPK Pharmaceuticals, Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	100 mL in 1 BOTTLE (53002-0100-2)
50090-3047-0	50090-3047	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20170612	N/A	ANDA	ANDA065089	A-S Medication Solutions	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	100 mL in 1 BOTTLE (50090-3047-0)
0093-2277-73	0093-2277	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20050113	N/A	ANDA	ANDA065089	Teva Pharmaceuticals USA, Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	200 mg/5mL; 28.5 mg/5mL	100 mL in 1 BOTTLE (0093-2277-73)
0093-2279-73	0093-2279	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20050113	N/A	ANDA	ANDA065089	Teva Pharmaceuticals USA, Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	100 mL in 1 BOTTLE (0093-2279-73)