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
57237-028-01	57237-028	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20051109	N/A	ANDA	ANDA065256	Rising Pharma Holdings, Inc.	AMOXICILLIN	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (57237-028-01)
57237-028-20	57237-028	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20051109	N/A	ANDA	ANDA065256	Rising Pharma Holdings, Inc.	AMOXICILLIN	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (57237-028-20)
65862-014-01	65862-014	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20051109	N/A	ANDA	ANDA065256	Aurobindo Pharma Limited	AMOXICILLIN	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-014-01)
65862-015-05	65862-015	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20051109	N/A	ANDA	ANDA065256	Aurobindo Pharma Limited	AMOXICILLIN	875 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-015-05)
65862-015-20	65862-015	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20051109	N/A	ANDA	ANDA065256	Aurobindo Pharma Limited	AMOXICILLIN	875 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (65862-015-20)
65862-014-20	65862-014	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20051109	N/A	ANDA	ANDA065256	Aurobindo Pharma Limited	AMOXICILLIN	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (65862-014-20)
65862-015-01	65862-015	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20051109	N/A	ANDA	ANDA065256	Aurobindo Pharma Limited	AMOXICILLIN	875 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-015-01)
65862-014-05	65862-014	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20051109	N/A	ANDA	ANDA065256	Aurobindo Pharma Limited	AMOXICILLIN	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-014-05)
70518-2191-1	70518-2191	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20190709	N/A	ANDA	ANDA065256	REMEDYREPACK INC.	AMOXICILLIN	875 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2191-1)
70518-2191-2	70518-2191	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20190719	N/A	ANDA	ANDA065256	REMEDYREPACK INC.	AMOXICILLIN	875 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-2)
70518-2191-3	70518-2191	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20190719	N/A	ANDA	ANDA065256	REMEDYREPACK INC.	AMOXICILLIN	875 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-3)
70518-2191-4	70518-2191	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20200708	N/A	ANDA	ANDA065256	REMEDYREPACK INC.	AMOXICILLIN	875 mg/1	14 TABLET, FILM COATED in 1 BLISTER PACK (70518-2191-4)