| JXHL0700231 | 盐酸羟考酮 | oxycodone hydrochloride | Active ingredient | Chemical Drugs(3.1) | Import Drug Application | 2007-08-22 | 威海路坦制药有限公司 | Weihai Lutan Pharmaceutical Co Ltd | Certificate Issued | 2008-06-27 | view |
| CXHS0601449 | 盐酸羟考酮 | oxycodone hydrochloride | Active ingredient | Chemical Drugs(4) | New Drug Application | 2007-03-14 | 北京四环医药科技股份有限公司 | Beijing Wellso Pharmaceutical Co Ltd | Certificate Issued | 2009-06-08 | view |
| JXHL0900187 | 盐酸羟考酮 | oxycodone hydrochloride | Active ingredient | Chemical Drugs | Import Drug Application | 2009-06-16 | 威海路坦制药有限公司 | Weihai Lutan Pharmaceutical Co Ltd | Certificate Issued | 2011-11-04 | view |
| CYHS1302078 | 盐酸羟考酮 | oxycodone hydrochloride | Active ingredient | Chemical Drugs(6) | Generic Drug | 2014-06-11 | 甘肃普瑞制药有限公司 | Alpine Dragon Pharmaceuticals Ltd | In Review | 2014-06-09 | view |
| CXL01415 | 盐酸羟考酮 | oxycodone hydrochloride | Active ingredient | Chemical Drugs(4) | New Drug Application | 2001-06-08 | 北京四环医药科技股份有限公司 | Beijing Wellso Pharmaceutical Co Ltd | Approval Completed-Pending Certificated | | view |
| JYHZ0800231 | 盐酸羟考酮控释片 | oxycodone hydrochloride | Tablet, extended release | Chemical Drugs | License Renew | 2008-09-03 | NAPP PHARMACEUTICALS LIMITED | Napp Pharmaceuticals Ltd | Certificate Issued | 2009-06-15 | view |
| JYHZ0800233 | 盐酸羟考酮控释片 | oxycodone hydrochloride | Tablet, extended release | Chemical Drugs | License Renew | 2008-09-03 | NAPP PHARMACEUTICALS LIMITED | Napp Pharmaceuticals Ltd | Certificate Issued | 2009-06-15 | view |
| JYHZ0800232 | 盐酸羟考酮控释片 | oxycodone hydrochloride | Tablet, extended release | Chemical Drugs | License Renew | 2008-09-03 | NAPP PHARMACEUTICALS LIMITED | Napp Pharmaceuticals Ltd | Certificate Issued | 2009-06-15 | view |
| JYHZ0800230 | 盐酸羟考酮控释片 | oxycodone hydrochloride | Tablet, extended release | Chemical Drugs | License Renew | 2008-09-03 | NAPP PHARMACEUTICALS LIMITED | Napp Pharmaceuticals Ltd | Certificate Issued | 2009-06-15 | view |
| JYHB2100164 | 盐酸羟考酮注射液 | oxycodone hydrochloride | Injection | Chemical Drugs | Supplementary Application | 2021-02-25 | 萌蒂(中国)制药有限公司 | Mundipharma (CHINA) Pharmaceutical Co Ltd | Certificate Issued | 2021-11-10 | view |
| CYHB2302223 | 盐酸羟考酮注射液 | oxycodone hydrochloride | Injection | Chemical Drugs(4) | Supplementary Application | 2023-10-09 | | Jiangsu Nhwa Pharmaceutical Co Ltd | | | view |
| JYHB1701209 | 盐酸羟考酮注射液 | oxycodone hydrochloride | Injection | Chemical Drugs | Supplementary Application | 2017-09-16 | 萌蒂(中国)制药有限公司 | Mundipharma (CHINA) Pharmaceutical Co Ltd | Filed | 2017-09-25 | view |
| JYHB1501205 | 盐酸羟考酮注射液 | oxycodone hydrochloride | Injection | Chemical Drugs | Supplementary Application | 2015-08-26 | 萌蒂（中国）制药有限公司 | Mundipharma (CHINA) Pharmaceutical Co Ltd | Certificate Issued | 2017-05-11 | view |
| JYHB2300092 | 盐酸羟考酮注射液 | oxycodone hydrochloride | Injection | Chemical Drugs | Supplementary Application | 2023-02-06 | | Napp Pharmaceuticals Ltd | | | view |
| JYHF1700119 | 盐酸羟考酮注射液 | oxycodone hydrochloride | Injection | Chemical Drugs | Supplementary Application | 2017-12-13 | NAPP PHARMACEUTICALS LIMITED | Napp Pharmaceuticals Ltd | Certificate Issued | 2018-01-29 | view |
| JYHB1600227 | 盐酸羟考酮注射液 | oxycodone hydrochloride | Injection | Chemical Drugs | Supplementary Application | 2016-03-10 | 萌蒂（中国）制药有限公司 | Mundipharma (CHINA) Pharmaceutical Co Ltd | Certificate Issued | 2017-01-04 | view |
| CYHS1900591 | 盐酸羟考酮注射液 | oxycodone hydrochloride | Injection | Chemical Drugs(4) | Generic Drug | 2019-08-17 | 北京华素制药股份有限公司 | Beijing Wellso Pharmaceutical Co Ltd | In Approval | 2021-11-23 | view |
| JYHB2400469 | 盐酸羟考酮注射液 | oxycodone hydrochloride | Injection | Chemical Drugs | Supplementary Application | 2024-08-30 | | Napp Pharmaceuticals Ltd | | | view |
| CYHS1700698 | 盐酸羟考酮注射液 | oxycodone hydrochloride | Injection | Chemical Drugs(4) | Generic Drug | 2018-06-13 | 江苏恩华药业股份有限公司 | Jiangsu Nhwa Pharmaceutical Co Ltd | Certificate Issued | 2021-03-03 | view |
| JYHB1400764 | 盐酸羟考酮注射液 | oxycodone hydrochloride | Injection | Chemical Drugs | Supplementary Application | 2014-06-16 | 萌蒂（中国）制药有限公司 | Mundipharma (CHINA) Pharmaceutical Co Ltd | Certificate Issued | 2014-12-11 | view |
