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
0093-4161-73	0093-4161	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20030226	N/A	ANDA	ANDA065119	Teva Pharmaceuticals USA, Inc.	AMOXICILLIN	400 mg/5mL	100 mL in 1 BOTTLE (0093-4161-73)
0093-4161-76	0093-4161	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20030701	N/A	ANDA	ANDA065119	Teva Pharmaceuticals USA, Inc.	AMOXICILLIN	400 mg/5mL	50 mL in 1 BOTTLE (0093-4161-76)
0093-4161-78	0093-4161	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20030701	N/A	ANDA	ANDA065119	Teva Pharmaceuticals USA, Inc.	AMOXICILLIN	400 mg/5mL	75 mL in 1 BOTTLE (0093-4161-78)
0093-4160-78	0093-4160	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20030701	N/A	ANDA	ANDA065119	Teva Pharmaceuticals USA, Inc.	AMOXICILLIN	200 mg/5mL	75 mL in 1 BOTTLE (0093-4160-78)
0093-4160-76	0093-4160	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20030701	N/A	ANDA	ANDA065119	Teva Pharmaceuticals USA, Inc.	AMOXICILLIN	200 mg/5mL	50 mL in 1 BOTTLE (0093-4160-76)
0093-4160-73	0093-4160	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20030402	N/A	ANDA	ANDA065119	Teva Pharmaceuticals USA, Inc.	AMOXICILLIN	200 mg/5mL	100 mL in 1 BOTTLE (0093-4160-73)
68788-8611-1	68788-8611	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20240320	N/A	ANDA	ANDA065119	Preferred Pharmaceuticals Inc.	AMOXICILLIN	200 mg/5mL	100 mL in 1 BOTTLE (68788-8611-1)
71205-177-00	71205-177	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20181201	N/A	ANDA	ANDA065119	Proficient Rx LP	AMOXICILLIN	400 mg/5mL	100 mL in 1 BOTTLE (71205-177-00)
68788-8731-1	68788-8731	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20240916	N/A	ANDA	ANDA065119	Preferred Pharmaceuticals Inc.	AMOXICILLIN	400 mg/5mL	100 mL in 1 BOTTLE (68788-8731-1)
53002-2369-3	53002-2369	HUMAN PRESCRIPTION DRUG	Amoxicillin	Amoxicillin	POWDER, FOR SUSPENSION	ORAL	20220101	N/A	ANDA	ANDA065119	RPK Pharmaceuticals, Inc.	AMOXICILLIN	400 mg/5mL	100 mL in 1 BOTTLE (53002-2369-3)