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
76420-762-20	76420-762	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20250108	N/A	ANDA	ANDA091490	Asclemed USA, Inc.	OXYCODONE HYDROCHLORIDE	30 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (76420-762-20)
76420-762-30	76420-762	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20250108	N/A	ANDA	ANDA091490	Asclemed USA, Inc.	OXYCODONE HYDROCHLORIDE	30 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (76420-762-30)
76420-762-60	76420-762	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20250108	N/A	ANDA	ANDA091490	Asclemed USA, Inc.	OXYCODONE HYDROCHLORIDE	30 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (76420-762-60)
72162-1334-6	72162-1334	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20240716	N/A	ANDA	ANDA091490	Bryant Ranch Prepack	OXYCODONE HYDROCHLORIDE	5 mg/1	60 TABLET in 1 BOTTLE (72162-1334-6)
72162-1334-9	72162-1334	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20240716	N/A	ANDA	ANDA091490	Bryant Ranch Prepack	OXYCODONE HYDROCHLORIDE	5 mg/1	90 TABLET in 1 BOTTLE (72162-1334-9)
72162-1334-2	72162-1334	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20240716	N/A	ANDA	ANDA091490	Bryant Ranch Prepack	OXYCODONE HYDROCHLORIDE	5 mg/1	20 TABLET in 1 BOTTLE (72162-1334-2)
76420-762-90	76420-762	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET	ORAL	20250108	N/A	ANDA	ANDA091490	Asclemed USA, Inc.	OXYCODONE HYDROCHLORIDE	30 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (76420-762-90)