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
43386-433-01	43386-433	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20170612	N/A	ANDA	ANDA204021	Lupin Pharmaceuticals,Inc.	OXYCODONE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (43386-433-01)
43386-434-01	43386-434	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20170612	N/A	ANDA	ANDA204021	Lupin Pharmaceuticals,Inc.	OXYCODONE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (43386-434-01)
43386-432-01	43386-432	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20170612	N/A	ANDA	ANDA204021	Lupin Pharmaceuticals,Inc.	OXYCODONE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (43386-432-01)
43386-431-01	43386-431	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20170612	N/A	ANDA	ANDA204021	Lupin Pharmaceuticals,Inc.	OXYCODONE HYDROCHLORIDE	30 mg/1	100 TABLET in 1 BOTTLE (43386-431-01)
43386-430-01	43386-430	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20170612	N/A	ANDA	ANDA204021	Lupin Pharmaceuticals,Inc.	OXYCODONE HYDROCHLORIDE	15 mg/1	100 TABLET in 1 BOTTLE (43386-430-01)
72189-095-30	72189-095	HUMAN PRESCRIPTION DRUG	OXYCODONE HYDROCHLORIDE	OXYCODONE HYDROCHLORIDE	TABLET	ORAL	20200615	N/A	ANDA	ANDA204021	DIRECT RX	OXYCODONE HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BOTTLE (72189-095-30)
72189-095-60	72189-095	HUMAN PRESCRIPTION DRUG	OXYCODONE HYDROCHLORIDE	OXYCODONE HYDROCHLORIDE	TABLET	ORAL	20200615	N/A	ANDA	ANDA204021	DIRECT RX	OXYCODONE HYDROCHLORIDE	5 mg/1	60 TABLET in 1 BOTTLE (72189-095-60)
72189-095-90	72189-095	HUMAN PRESCRIPTION DRUG	OXYCODONE HYDROCHLORIDE	OXYCODONE HYDROCHLORIDE	TABLET	ORAL	20200615	N/A	ANDA	ANDA204021	DIRECT RX	OXYCODONE HYDROCHLORIDE	5 mg/1	90 TABLET in 1 BOTTLE (72189-095-90)