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
50090-0713-1	50090-0713	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20180606	N/A	ANDA	ANDA065256	A-S Medication Solutions	AMOXICILLIN	875 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (50090-0713-1)
50090-0713-2	50090-0713	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA065256	A-S Medication Solutions	AMOXICILLIN	875 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-0713-2)
68071-4982-2	68071-4982	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20190724	N/A	ANDA	ANDA065256	NuCare Pharmaceuticals,Inc.	AMOXICILLIN	875 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68071-4982-2)
63187-729-30	63187-729	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20160801	N/A	ANDA	ANDA065256	Proficient Rx LP	AMOXICILLIN	875 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-729-30)
63187-729-40	63187-729	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20160801	N/A	ANDA	ANDA065256	Proficient Rx LP	AMOXICILLIN	875 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (63187-729-40)
70934-038-14	70934-038	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20191014	20250731	ANDA	ANDA065256	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	AMOXICILLIN	875 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-038-14)
70934-038-20	70934-038	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20181130	20250731	ANDA	ANDA065256	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	AMOXICILLIN	875 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-038-20)
70934-038-91	70934-038	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20171031	20250731	ANDA	ANDA065256	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	AMOXICILLIN	875 mg/1	20 TABLET, FILM COATED in 1 DOSE PACK (70934-038-91)
70934-038-94	70934-038	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20171031	20250731	ANDA	ANDA065256	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	AMOXICILLIN	875 mg/1	30 TABLET, FILM COATED in 1 DOSE PACK (70934-038-94)
53002-0130-1	53002-0130	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20171001	N/A	ANDA	ANDA065256	RPK Pharmaceuticals, Inc.	AMOXICILLIN	875 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (53002-0130-1)
53002-0130-2	53002-0130	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20171001	N/A	ANDA	ANDA065256	RPK Pharmaceuticals, Inc.	AMOXICILLIN	875 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (53002-0130-2)
53002-0170-2	53002-0170	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA065256	RPK Pharmaceuticals, Inc.	AMOXICILLIN	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (53002-0170-2)
61919-135-20	61919-135	HUMAN PRESCRIPTION DRUG	AMOXIL	AMOXICILLIN	TABLET, FILM COATED	ORAL	20160708	N/A	ANDA	ANDA065256	DIRECT RX	AMOXICILLIN	875 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (61919-135-20)