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
59011-415-20	59011-415	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	15 mg/1	2 BLISTER PACK in 1 CARTON (59011-415-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
59011-420-10	59011-420	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-420-10)
59011-420-20	59011-420	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	20 mg/1	2 BLISTER PACK in 1 CARTON (59011-420-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
59011-430-10	59011-430	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	30 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-430-10)
59011-415-10	59011-415	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	15 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-415-10)
59011-410-20	59011-410	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	10 mg/1	2 BLISTER PACK in 1 CARTON (59011-410-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
59011-410-10	59011-410	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-410-10)
59011-460-10	59011-460	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	60 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-460-10)
59011-460-20	59011-460	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	60 mg/1	2 BLISTER PACK in 1 CARTON (59011-460-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
59011-480-10	59011-480	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	80 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-480-10)
59011-480-20	59011-480	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	80 mg/1	2 BLISTER PACK in 1 CARTON (59011-480-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
59011-430-20	59011-430	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	30 mg/1	2 BLISTER PACK in 1 CARTON (59011-430-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
59011-440-10	59011-440	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-440-10)
59011-440-20	59011-440	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Knoa Pharma LLC	OXYCODONE HYDROCHLORIDE	40 mg/1	2 BLISTER PACK in 1 CARTON (59011-440-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
0115-1560-01	0115-1560	HUMAN PRESCRIPTION DRUG	OXYCODONE HYDROCHLORIDE	OXYCODONE HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160222	N/A	NDA AUTHORIZED GENERIC	NDA022272	Amneal Pharmaceuticals of New York LLC	OXYCODONE HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0115-1560-01)