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
0781-1874-31	0781-1874	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20050823	N/A	ANDA	ANDA065189	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/1; 125 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0781-1874-31)
70882-111-20	70882-111	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20050823	N/A	ANDA	ANDA065189	Cambridge Therapeutics Technologies, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/1; 125 mg/1	20 TABLET, FILM COATED in 1 BLISTER PACK (70882-111-20)
16714-476-01	16714-476	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20151101	N/A	ANDA	ANDA065189	Northstar RxLLC	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/1; 125 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16714-476-01)
76420-503-30	76420-503	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	TABLET, FILM COATED	ORAL	20191015	N/A	ANDA	ANDA065189	Asclemed USA, Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/1; 125 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-503-30)