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
81964-220-28	81964-220	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20251215	N/A	NDA AUTHORIZED GENERIC	NDA050785	USAntibiotics, LLC	AMOXICILLIN; AMOXICILLIN SODIUM; CLAVULANATE POTASSIUM	562.5 mg/1; 437.5 mg/1; 62.5 mg/1	28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (81964-220-28)
81964-220-40	81964-220	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	amoxicillin and clavulanate potassium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20251215	N/A	NDA AUTHORIZED GENERIC	NDA050785	USAntibiotics, LLC	AMOXICILLIN; AMOXICILLIN SODIUM; CLAVULANATE POTASSIUM	562.5 mg/1; 437.5 mg/1; 62.5 mg/1	40 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (81964-220-40)