Menovo subsidiary passes first US FDA on-site inspection for tildipirosin API
November 6, 2026
Source: drugdu
52
Menovo (603538) disclosed on November 6 that its controlled subsidiary, Xuancheng Menovo, received a US FDA inspection report on November 4 confirming that it had passed its first FDA on-site inspection for tildipirosin API. The preapproval cGMP inspection ran from June 22 to 26, 2026, and covered quality, materials, manufacturing, facilities and equipment, packaging and labeling, and laboratory controls.
The company said the inspection outcome would support its international expansion. Menovo develops, manufactures and sells specialty APIs and finished dosage forms. In the first nine months of 2026, revenue rose 29.00% year on year to RMB 1.441 billion, and net profit attributable to shareholders rose 8.54% to RMB 104 million.
Source: http://finance.eastmoney.com/a/202611063924413520.html
Copyright©2026 Ddu. All rights reserved.
Read more on
- Boyi Group completes nearly 100 million RMB Series B financing November 6, 2026
- Net profit surges by 588%! A century-old traditional Chinese medicine brand successfully shifts gears. November 6, 2026
- Singapore approves CMS’s ruxolitinib phosphate cream for nonsegmental vitiligo November 6, 2026
- China accepts United Laboratories’ semaglutide injection filing for weight management November 6, 2026
- Daridorexant receives US FDA Breakthrough Therapy designation for pediatric insomnia November 6, 2026
your submission has already been received.
OK
Subscribe
Please enter a valid Email address！
Submit
The most relevant industry news & insight will be sent to you every two weeks.
