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Viwit 2025 Annual Shareholders’ Meeting Successfully Concluded | Focus on Innovation, Steady Progress
39th World No Tobacco Day | Smoke-Free Youth, Boundless Future — Science-Based Smoking Cessation Makes Health and Future Accessible
Viwit’s Video “Ten Years in China, Growing with Viwit” Wins Second Prize in 2025 Shandong Province Foreign Expert Video Competition
Viwit Wins JD.com “Innovation Marketing Award” | Dr. Keene Wei Invited to JD Health 10th Anniversary & 2026 JD Pharmacy Partner Conference
Dr. Keene Wei Named “Outstanding Entrepreneur” by Both Tengzhou City and Zaozhuang High-Tech Zone
Dr. Keene Wei Invited as Keynote Speaker at His Alma Mater Dartmouth College’s Dreyfus Lecture, Showcasing Chinese Pharmaceutical Innovation
Viwit Pharmaceuticals' Bimatoprost Eye Drops Receive Official Approval by China NMPA
Recently, Viwit Pharmaceuticals received the "Drug registration certificate" issued by China National Medical Products Administration (NMPA) for Bimatoprost Eye Drops. The approval number is H20244103. This signifies that the product has received official approval for the Chinese market and has successfully passed the generic drug consistency evaluation, thereby becoming the second domestic generic drug of its kind.
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Viwit Pharmaceuticals' Gadoterate Meglumine Injection Receives Official Approval by China NMPA
Viwit Pharmaceuticals proudly announces the receipt of the "Drug Supplementary Application Approval Notice" from the National Medical Products Administration (NMPA) for their Gadoterate Meglumine Injection. This approval includes the following strengths: 10 mL containing 3.769 g, 15 mL containing 5.654 g, and 20 mL containing 7.538 g. The corresponding approval numbers are H20243899, H20243900, and H20243901.
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Viwit Pharmaceuticals' Deslanoside Injection Receives Official Approval by China NMPA
May 8, 2024 – Viwit Pharmaceuticals proudly announces the receipt of the "Drug Supplementary Application Approval Notice" from the National Medical Products Administration (NMPA) for the drug product, Deslanoside Injection. The approval notice number is 2024B01980.
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Viwit’s Levetiracetam Tablets Approved by FDA
On April 5, 2024, Viwit Pharmaceuticals' Levetiracetam Tablets received an Approval Letter (#078869) from the U.S. Food and Drug Administration (FDA), marking Viwit's first approved oral solid dosage in the United States.
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Viwit Pharmaceuticals' Mirabegron API Receives Official Approval by China NMPA
On January 23, 2024, Viwit Pharmaceuticals received the "Notice of Approval of Application for Listing of Chemical APIs" issued by China National Medical Products Administration (NMPA) for its own proprietary active pharmaceutical ingredient (API) Mirabegron, developed independently. The issued registration number is Y20220000096, and the corresponding notice number is 2024YS00039.
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