| CYHS2403508 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(3) | Generic Drug | 2024-10-17 | | | | | view |
| CYHS2200865 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(3) | Generic Drug | 2022-06-13 | | Hainan Huigu Pharmaceutical Co Ltd | | | view |
| CYHB2300784 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(原5) | Supplementary Application | 2023-04-15 | | Chengdu Kanghong Pharmaceutical Group Co Ltd | | | view |
| CYHS2101794 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(3) | Generic Drug | 2021-09-29 | | Hefei Lifeon Pharmaceutical Co Ltd | | | view |
| CYHB2300549 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(3) | Supplementary Application | 2023-03-16 | | | | | view |
| CYHB2101511 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(3) | Supplementary Application | 2021-07-08 | | | | | view |
| CYHB2300376 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(原5) | Supplementary Application | 2023-02-23 | | Chengdu Kanghong Pharmaceutical Group Co Ltd | | | view |
| JXHL1300090 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs | Import Drug Application | 2013-04-01 | DALT PHARMA, S.A. | Dalt Pharma SA | Certificate Issued | 2015-11-27 | view |
| JXHL1300091 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs | Import Drug Application | 2013-03-27 | DALT PHARMA, S.A. | Dalt Pharma SA | Certificate Issued | 2015-11-27 | view |
| CXHL0800065 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(5) | New Drug Application | 2008-03-21 | 上海医药科技发展有限公司 | Shanghai Medicine Science & Technology Development Co Ltd | Certificate Issued | 2009-05-05 | view |
| JXHL1100054 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs | Import Drug Application | 2011-03-07 | 印度太阳药业有限公司 | Sun Pharmaceutical Industries Ltd | Certificate Issued | 2015-11-27 | view |
| JXHL1100056 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs | Import Drug Application | 2011-03-07 | 印度太阳药业有限公司 | Sun Pharmaceutical Industries Ltd | Certificate Issued | 2015-11-27 | view |
| JXHL1100051 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs | Import Drug Application | 2011-03-18 | 印度太阳药业有限公司 | Sun Pharmaceutical Industries Ltd | Certificate Issued | 2015-11-27 | view |
| CXHL0700226 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(5) | New Drug Application | 2007-08-22 | 合肥立方制药有限公司 | Hefei Lifeon Pharmaceutical Co Ltd | Certificate Issued | 2009-02-06 | view |
| CXHS1300057 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(5) | New Drug Application | 2013-09-06 | 合肥立方制药股份有限公司 | Hefei Lifeon Pharmaceutical Co Ltd | Certificate Issued | 2016-05-19 | view |
| CYHS1401581 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(6) | Generic Drug | 2015-04-30 | 合肥英太制药有限公司 | Hefei Yingtai Pharmaceutical Co Ltd | Certificate Issued | 2016-03-01 | view |
| CYHS1501374 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(6) | Generic Drug | 2016-03-07 | 国药集团国瑞药业有限公司 | China National Medicines Guorui Pharmaceutical Co Ltd | Certificate Issued | 2016-10-27 | view |
| CYHS1900540 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs(3) | Generic Drug | 2019-07-30 | 国药集团国瑞药业有限公司 | China National Medicines Guorui Pharmaceutical Co Ltd | Certificate Issued | 2021-01-08 | view |
| CYHB1850451 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs | Supplementary Application | 2019-01-09 | 成都康弘药业集团股份有限公司 | Chengdu Kanghong Pharmaceutical Group Co Ltd | Certificate Issued | 2019-11-05 | view |
| CYHB1110183 | 盐酸文拉法辛缓释片 | venlafaxine hydrochloride | Tablet, extended release | Chemical Drugs | Supplementary Application | 2011-11-21 | 成都康弘药业集团股份有限公司 | Chengdu Kanghong Pharmaceutical Group Co Ltd | Certificate Issued | 2012-08-06 | view |
