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
0781-6102-46	0781-6102	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20020605	N/A	ANDA	ANDA065066	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	200 mg/5mL; 28.5 mg/5mL	100 mL in 1 BOTTLE (0781-6102-46)
0781-6102-57	0781-6102	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20231218	N/A	ANDA	ANDA065066	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	200 mg/5mL; 28.5 mg/5mL	75 mL in 1 BOTTLE (0781-6102-57)
0781-6104-46	0781-6104	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20020605	N/A	ANDA	ANDA065066	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	100 mL in 1 BOTTLE (0781-6104-46)
0781-6104-52	0781-6104	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20231218	N/A	ANDA	ANDA065066	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	50 mL in 1 BOTTLE (0781-6104-52)
0781-6104-57	0781-6104	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20231218	N/A	ANDA	ANDA065066	Sandoz Inc	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	75 mL in 1 BOTTLE (0781-6104-57)
68788-8000-1	68788-8000	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20210810	N/A	ANDA	ANDA065066	Preferred Pharmaceuticals Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	200 mg/5mL; 28.5 mg/5mL	100 mL in 1 BOTTLE (68788-8000-1)
69452-335-43	69452-335	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20220801	N/A	ANDA	ANDA065066	Bionpharma Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	100 mL in 1 BOTTLE (69452-335-43)
69452-334-43	69452-334	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20220801	N/A	ANDA	ANDA065066	Bionpharma Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	200 mg/5mL; 28.5 mg/5mL	100 mL in 1 BOTTLE (69452-334-43)
68071-5216-1	68071-5216	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20200318	N/A	ANDA	ANDA065066	NuCare Pharmaceuticals,Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	200 mg/5mL; 28.5 mg/5mL	100 mL in 1 BOTTLE (68071-5216-1)
68788-8305-1	68788-8305	HUMAN PRESCRIPTION DRUG	Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	POWDER, FOR SUSPENSION	ORAL	20221219	N/A	ANDA	ANDA065066	Preferred Pharmaceuticals Inc.	AMOXICILLIN; CLAVULANATE POTASSIUM	400 mg/5mL; 57 mg/5mL	100 mL in 1 BOTTLE (68788-8305-1)