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
72189-463-20	72189-463	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20230417	N/A	ANDA	ANDA065228	Direct_Rx	AMOXICILLIN	875 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (72189-463-20)
71205-035-30	71205-035	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20180501	N/A	ANDA	ANDA065228	Proficient Rx LP	AMOXICILLIN	875 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-035-30)
71205-035-90	71205-035	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20180501	N/A	ANDA	ANDA065228	Proficient Rx LP	AMOXICILLIN	875 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-035-90)
71205-035-20	71205-035	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20180501	N/A	ANDA	ANDA065228	Proficient Rx LP	AMOXICILLIN	875 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71205-035-20)
71205-035-14	71205-035	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA065228	Proficient Rx LP	AMOXICILLIN	875 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71205-035-14)
71205-035-60	71205-035	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20180501	N/A	ANDA	ANDA065228	Proficient Rx LP	AMOXICILLIN	875 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-035-60)
0781-5061-01	0781-5061	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20050713	N/A	ANDA	ANDA065228	Sandoz Inc	AMOXICILLIN	875 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0781-5061-01)
0781-5061-20	0781-5061	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	TABLET, FILM COATED	ORAL	20050713	N/A	ANDA	ANDA065228	Sandoz Inc	AMOXICILLIN	875 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (0781-5061-20)