| Acceptance No. | Drug Name | Active Ingredient | Dosage Form | Classification | Submission | Acceptance Date | Manufacturers | Manufacturers | Review Status | Status Date | View |
|---|---|---|---|---|---|---|---|---|---|---|---|
| CXHL0601035 | 盐酸度洛西汀缓释片 | duloxetine hydrochloride | Tablet, extended release | Chemical Drugs(3.1) | New Drug Application | 2006-10-27 | 重庆圣华曦药业有限公司 | Chongqing Shenghuaxi Pharmaceutical Ltd | Certificate Issued | 2009-03-02 | view |