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
60687-406-67	60687-406	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	SOLUTION	ORAL	20190322	N/A	ANDA	ANDA204037	American Health Packaging	OXYCODONE HYDROCHLORIDE	5 mg/5mL	5 TRAY in 1 CASE (60687-406-67) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-406-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-406-40)
60687-406-77	60687-406	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	SOLUTION	ORAL	20190322	N/A	ANDA	ANDA204037	American Health Packaging	OXYCODONE HYDROCHLORIDE	5 mg/5mL	4 TRAY in 1 CASE (60687-406-77) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-406-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-406-40)
17856-0390-2	17856-0390	HUMAN PRESCRIPTION DRUG	oxycodone hydrochloride	oxycodone hydrochloride	SOLUTION	ORAL	20240515	N/A	ANDA	ANDA204037	ATLANTIC BIOLOGICALS CORP.	OXYCODONE HYDROCHLORIDE	5 mg/5mL	1 CUP, UNIT-DOSE in 1 CUP, UNIT-DOSE (17856-0390-2) / 5 CUP, UNIT-DOSE in 1 CUP, UNIT-DOSE (17856-0390-3) / 72 CUP, UNIT-DOSE in 1 CUP, UNIT-DOSE (17856-0390-1) / 5 mL in 1 CUP, UNIT-DOSE
0054-0390-63	0054-0390	HUMAN PRESCRIPTION DRUG	oxycodone hydrochloride	oxycodone hydrochloride	SOLUTION	ORAL	20140904	N/A	ANDA	ANDA204037	Hikma Pharmceuticals USA Inc.	OXYCODONE HYDROCHLORIDE	5 mg/5mL	500 mL in 1 BOTTLE (0054-0390-63)
0054-0390-41	0054-0390	HUMAN PRESCRIPTION DRUG	oxycodone hydrochloride	oxycodone hydrochloride	SOLUTION	ORAL	20140904	N/A	ANDA	ANDA204037	Hikma Pharmceuticals USA Inc.	OXYCODONE HYDROCHLORIDE	5 mg/5mL	15 mL in 1 BOTTLE (0054-0390-41)