美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=OXYCONTIN"
符合检索条件的记录共 7 条
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商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
OXYCONTIN 022272 001 NDA OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 10MG Yes No 2010/04/05 2010/04/05 PURDUE PHARMA LP Prescription
OXYCONTIN 022272 002 NDA OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 15MG Yes No 2010/04/05 2010/04/05 PURDUE PHARMA LP Prescription
OXYCONTIN 022272 003 NDA OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 20MG Yes No 2010/04/05 2010/04/05 PURDUE PHARMA LP Prescription
OXYCONTIN 022272 004 NDA OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 30MG Yes No 2010/04/05 2010/04/05 PURDUE PHARMA LP Prescription
OXYCONTIN 022272 005 NDA OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 40MG Yes Yes 2010/04/05 2010/04/05 PURDUE PHARMA LP Prescription
OXYCONTIN 022272 006 NDA OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 60MG Yes No 2010/04/05 2010/04/05 PURDUE PHARMA LP Prescription
OXYCONTIN 022272 007 NDA OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 80MG Yes No 2010/04/05 2010/04/05 PURDUE PHARMA LP Prescription
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