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）
检索条件:" 注册申请号=NDA022272"
符合检索条件的记录共 18 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
59011-430-10 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
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)
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
59011-440-10 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
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)
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)
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
59011-480-10 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)
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
59011-460-10 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
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