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Viwit Pharmaceutical’s Lifitegrast API has completed registrations in both China and the US! 2024-08-14 11:55:51
Recently, Viwit Pharmaceutical’s self-developed Lifitegrast API has completed the registrations in China and the United States. The API registration number is Y20240000726, and the US DMF number is 040172.
Viwit Pharmaceutical's Varenicline Tartrate Tablet receives official approval from South Africa 2024-07-15 10:01:41
Recently, theViwit independently developed smoking cessation drug Varenicline (Tartrate) Tablets, in strengths of 0.5 mg and 1 mg, received the Drug Registration Certificate issued by the South African Health Products Regulatory Authority (SAHPRA).
Viwit Pharmaceutical's Fosaprepitant Dimeglumine API Receives Official Approval from NMPA 2024-07-12 09:12:19
On July 5, 2024, Viwit Pharmaceitical’s independently developed Fosaprepitant Dimeglumine API received the "Notice of Approval of Application for Listing of Chemical APIs" issued by National Medical Products Administration (NMPA). The registration number is Y20220000736, and the notice number is 2024YS00664.
Viwit Pharmaceuticals' Bimatoprost Eye Drops Receive Official Approval by China NMPA 2024-07-09 10:54:01
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.
Viwit Pharmaceuticals' Gadoterate Meglumine Injection Receives Official Approval by China NMPA 2024-06-17 15:13:15
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.
Viwit Pharmaceuticals' Deslanoside Injection Receives Official Approval by China NMPA 2024-06-15 10:26:00
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.

In 2024

08-14

Viwit Pharmaceutical’s Lifitegrast API has completed registrations in both China and the US!

Recently, Viwit Pharmaceutical’s self-developed Lifitegrast API has completed the registrations in China and the United States. The API registration number is Y20240000726, and the US DMF number is 040172.
Viwit Pharmaceutical’s Lifitegrast API has completed registrations in both China and the US!
07-15

Viwit Pharmaceutical's Varenicline Tartrate Tablet receives official approval from South Africa

Recently, theViwit independently developed smoking cessation drug Varenicline (Tartrate) Tablets, in strengths of 0.5 mg and 1 mg, received the Drug Registration Certificate issued by the South African Health Products Regulatory Authority (SAHPRA).
Viwit Pharmaceutical's Varenicline Tartrate Tablet receives official approval from South Africa
07-12

Viwit Pharmaceutical's Fosaprepitant Dimeglumine API Receives Official Approval from NMPA

On July 5, 2024, Viwit Pharmaceitical’s independently developed Fosaprepitant Dimeglumine API received the "Notice of Approval of Application for Listing of Chemical APIs" issued by National Medical Products Administration (NMPA). The registration number is Y20220000736, and the notice number is 2024YS00664.
Viwit Pharmaceutical's Fosaprepitant Dimeglumine API Receives Official Approval from NMPA
07-09

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.
Viwit Pharmaceuticals' Bimatoprost Eye Drops Receive Official Approval by China NMPA
06-17

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.
Viwit Pharmaceuticals' Gadoterate Meglumine Injection Receives Official Approval by China NMPA
06-15

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.
Viwit Pharmaceuticals' Deslanoside Injection Receives Official Approval by China NMPA
04-09

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.
Viwit’s Levetiracetam Tablets Approved by FDA
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