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
71297-240-36	71297-240	HUMAN PRESCRIPTION DRUG	Augmentin	Amoxicillin and Clavulanate Potassium	FOR SUSPENSION	ORAL	20230901	N/A	NDA	NDA050575	Allegis Holdings, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	125 mg/5mL; 31.25 mg/5mL	150 mL in 1 BOTTLE (71297-240-36)
71297-240-35	71297-240	HUMAN PRESCRIPTION DRUG	Augmentin	Amoxicillin and Clavulanate Potassium	FOR SUSPENSION	ORAL	20230901	N/A	NDA	NDA050575	Allegis Holdings, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	125 mg/5mL; 31.25 mg/5mL	100 mL in 1 BOTTLE (71297-240-35)
71297-240-34	71297-240	HUMAN PRESCRIPTION DRUG	Augmentin	Amoxicillin and Clavulanate Potassium	FOR SUSPENSION	ORAL	20240220	N/A	NDA	NDA050575	Allegis Holdings, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	125 mg/5mL; 31.25 mg/5mL	75 mL in 1 BOTTLE (71297-240-34)
28595-240-35	28595-240	HUMAN PRESCRIPTION DRUG	Augmentin	Amoxicillin and Clavulanate Potassium	FOR SUSPENSION	ORAL	20230223	N/A	NDA	NDA050575	Allegis Pharmaceuticals, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	125 mg/5mL; 31.25 mg/5mL	100 mL in 1 BOTTLE (28595-240-35)
28595-240-36	28595-240	HUMAN PRESCRIPTION DRUG	Augmentin	Amoxicillin and Clavulanate Potassium	FOR SUSPENSION	ORAL	20230223	N/A	NDA	NDA050575	Allegis Pharmaceuticals, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	125 mg/5mL; 31.25 mg/5mL	150 mL in 1 BOTTLE (28595-240-36)
81964-204-15	81964-204	HUMAN PRESCRIPTION DRUG	AMOXICILLIN AND CLAVULANATE POTASSIUM	Amoxicillin and Clavulanate Potassium	FOR SUSPENSION	ORAL	20221205	N/A	NDA AUTHORIZED GENERIC	NDA050575	USAntibiotics, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/5mL; 62.5 mg/5mL	150 mL in 1 BOTTLE (81964-204-15)
81964-212-03	81964-212	HUMAN PRESCRIPTION DRUG	AMOXICILLIN AND CLAVULANATE POTASSIUM	Amoxicillin and Clavulanate Potassium	FOR SUSPENSION	ORAL	20221205	N/A	NDA AUTHORIZED GENERIC	NDA050575	USAntibiotics, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	125 mg/5mL; 31.25 mg/5mL	100 mL in 1 BOTTLE (81964-212-03)
81964-212-05	81964-212	HUMAN PRESCRIPTION DRUG	AMOXICILLIN AND CLAVULANATE POTASSIUM	Amoxicillin and Clavulanate Potassium	FOR SUSPENSION	ORAL	20221205	N/A	NDA AUTHORIZED GENERIC	NDA050575	USAntibiotics, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	125 mg/5mL; 31.25 mg/5mL	150 mL in 1 BOTTLE (81964-212-05)
81964-212-01	81964-212	HUMAN PRESCRIPTION DRUG	AMOXICILLIN AND CLAVULANATE POTASSIUM	Amoxicillin and Clavulanate Potassium	FOR SUSPENSION	ORAL	20221205	N/A	NDA AUTHORIZED GENERIC	NDA050575	USAntibiotics, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	125 mg/5mL; 31.25 mg/5mL	75 mL in 1 BOTTLE (81964-212-01)
81964-204-07	81964-204	HUMAN PRESCRIPTION DRUG	AMOXICILLIN AND CLAVULANATE POTASSIUM	Amoxicillin and Clavulanate Potassium	FOR SUSPENSION	ORAL	20221205	N/A	NDA AUTHORIZED GENERIC	NDA050575	USAntibiotics, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/5mL; 62.5 mg/5mL	75 mL in 1 BOTTLE (81964-204-07)
81964-204-10	81964-204	HUMAN PRESCRIPTION DRUG	AMOXICILLIN AND CLAVULANATE POTASSIUM	Amoxicillin and Clavulanate Potassium	FOR SUSPENSION	ORAL	20221205	N/A	NDA AUTHORIZED GENERIC	NDA050575	USAntibiotics, LLC	AMOXICILLIN; CLAVULANATE POTASSIUM	250 mg/5mL; 62.5 mg/5mL	100 mL in 1 BOTTLE (81964-204-10)