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
59011-410-10	59011-410	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Purdue Pharma LP	OXYCODONE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-410-10)
59011-410-20	59011-410	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Purdue Pharma LP	OXYCODONE HYDROCHLORIDE	10 mg/1	2 BLISTER PACK in 1 CARTON (59011-410-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
59011-415-10	59011-415	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Purdue Pharma LP	OXYCODONE HYDROCHLORIDE	15 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-415-10)
59011-415-20	59011-415	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Purdue Pharma LP	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	Purdue Pharma LP	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	Purdue Pharma LP	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	Purdue Pharma LP	OXYCODONE HYDROCHLORIDE	30 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-430-10)
59011-430-20	59011-430	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Purdue Pharma LP	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	Purdue Pharma LP	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	Purdue Pharma LP	OXYCODONE HYDROCHLORIDE	40 mg/1	2 BLISTER PACK in 1 CARTON (59011-440-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
59011-460-10	59011-460	HUMAN PRESCRIPTION DRUG	OxyContin	oxycodone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20100808	N/A	NDA	NDA022272	Purdue Pharma LP	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	Purdue Pharma LP	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	Purdue Pharma LP	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	Purdue Pharma LP	OXYCODONE HYDROCHLORIDE	80 mg/1	2 BLISTER PACK in 1 CARTON (59011-480-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
69238-2294-1	69238-2294	HUMAN PRESCRIPTION DRUG	Oxycodone HCl	Oxycodone HCl	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220401	N/A	NDA AUTHORIZED GENERIC	NDA022272	Amneal Pharmaceuticals NY LLC	OXYCODONE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2294-1)
69238-2296-1	69238-2296	HUMAN PRESCRIPTION DRUG	Oxycodone HCl	Oxycodone HCl	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220401	N/A	NDA AUTHORIZED GENERIC	NDA022272	Amneal Pharmaceuticals NY LLC	OXYCODONE HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2296-1)
69238-2298-1	69238-2298	HUMAN PRESCRIPTION DRUG	Oxycodone HCl	Oxycodone HCl	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220401	N/A	NDA AUTHORIZED GENERIC	NDA022272	Amneal Pharmaceuticals NY LLC	OXYCODONE HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2298-1)
69238-2300-1	69238-2300	HUMAN PRESCRIPTION DRUG	Oxycodone HCl	Oxycodone HCl	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220401	N/A	NDA AUTHORIZED GENERIC	NDA022272	Amneal Pharmaceuticals NY LLC	OXYCODONE HYDROCHLORIDE	80 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2300-1)
0093-5731-01	0093-5731	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20151012	20241231	NDA AUTHORIZED GENERIC	NDA022272	Teva Pharmaceuticals USA, Inc.	OXYCODONE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5731-01)
0093-5732-01	0093-5732	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride	Oxycodone Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20151012	20241231	NDA AUTHORIZED GENERIC	NDA022272	Teva Pharmaceuticals USA, Inc.	OXYCODONE HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5732-01)