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
76420-764-05	76420-764	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20240625	N/A	ANDA	ANDA202116	Asclemed USA, Inc.	OXYCODONE HYDROCHLORIDE	15 mg/1	500 TABLET in 1 BOTTLE (76420-764-05)
76420-764-10	76420-764	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20240625	N/A	ANDA	ANDA202116	Asclemed USA, Inc.	OXYCODONE HYDROCHLORIDE	15 mg/1	10 TABLET in 1 BOTTLE (76420-764-10)
76420-764-20	76420-764	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20240625	N/A	ANDA	ANDA202116	Asclemed USA, Inc.	OXYCODONE HYDROCHLORIDE	15 mg/1	20 TABLET in 1 BOTTLE (76420-764-20)
76420-764-30	76420-764	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20240625	N/A	ANDA	ANDA202116	Asclemed USA, Inc.	OXYCODONE HYDROCHLORIDE	15 mg/1	30 TABLET in 1 BOTTLE (76420-764-30)
76420-764-60	76420-764	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20240625	N/A	ANDA	ANDA202116	Asclemed USA, Inc.	OXYCODONE HYDROCHLORIDE	15 mg/1	60 TABLET in 1 BOTTLE (76420-764-60)
76420-764-90	76420-764	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20240625	N/A	ANDA	ANDA202116	Asclemed USA, Inc.	OXYCODONE HYDROCHLORIDE	15 mg/1	90 TABLET in 1 BOTTLE (76420-764-90)
47781-265-01	47781-265	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20111230	N/A	ANDA	ANDA202116	Alvogen, Inc.	OXYCODONE HYDROCHLORIDE	30 mg/1	100 TABLET in 1 BOTTLE (47781-265-01)
47781-265-05	47781-265	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20111230	N/A	ANDA	ANDA202116	Alvogen, Inc.	OXYCODONE HYDROCHLORIDE	30 mg/1	500 TABLET in 1 BOTTLE (47781-265-05)