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
63629-8890-1	63629-8890	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20211011	N/A	ANDA	ANDA207418	Bryant Ranch Prepack	OXYCODONE HYDROCHLORIDE	30 mg/1	30 TABLET in 1 BOTTLE (63629-8890-1)
63629-8890-2	63629-8890	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20211011	N/A	ANDA	ANDA207418	Bryant Ranch Prepack	OXYCODONE HYDROCHLORIDE	30 mg/1	60 TABLET in 1 BOTTLE (63629-8890-2)
63629-8890-3	63629-8890	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20211011	N/A	ANDA	ANDA207418	Bryant Ranch Prepack	OXYCODONE HYDROCHLORIDE	30 mg/1	90 TABLET in 1 BOTTLE (63629-8890-3)
63629-8890-4	63629-8890	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20211011	N/A	ANDA	ANDA207418	Bryant Ranch Prepack	OXYCODONE HYDROCHLORIDE	30 mg/1	120 TABLET in 1 BOTTLE (63629-8890-4)
31722-917-01	31722-917	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20170808	N/A	ANDA	ANDA207418	Camber Pharmaceuticals Inc	OXYCODONE HYDROCHLORIDE	15 mg/1	100 TABLET in 1 BOTTLE (31722-917-01)
31722-917-05	31722-917	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20170808	N/A	ANDA	ANDA207418	Camber Pharmaceuticals Inc	OXYCODONE HYDROCHLORIDE	15 mg/1	500 TABLET in 1 BOTTLE (31722-917-05)