Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
01 1Cayman Pharma sro
02 1MSN Laboratories Private Limited
03 1NEWCHEM SPA
04 1YS Life Science Co., Ltd.
01 1Clasia Co., Ltd.
02 1MPK Korea Co., Ltd.
03 1Sungjin Exim Co., Ltd.
04 1YS Life Science Co., Ltd.
01 4Latanoprostinod
01 1Czech Republic
02 1India
03 1Italy
04 1South Korea
Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
Registrant Name : Clasia Co., Ltd.
Registration Date : 2024-01-15
Registration Number : Su758-10-ND
Manufacturer Name : Cayman Pharma sro
Manufacturer Address : Práce 657, 277 11 Neratovice, Czech Republic
Registrant Name : MPK Korea Co., Ltd.
Registration Date : 2025-02-28
Registration Number : Su812-25-ND
Manufacturer Name : MSN Laboratories Private Lim...
Manufacturer Address : (Unit-ll) Sy. No. 50, 53, 53/A, 54 & 54/A, Kardanur (Village), Patancheru (Mandal), S...
Registrant Name : Sungjin Exim Co., Ltd.
Registration Date : 2025-11-07
Registration Number : Su133-23-ND
Manufacturer Name : NEWCHEM SPA
Manufacturer Address : Via Parco del Ticino, 10-27100 San Martino Siccomario-Pavia Italy
Registrant Name : YS Life Science Co., Ltd.
Registration Date : 2024-10-09
Registration Number : 2247-1-ND
Manufacturer Name : YS Life Science Co., Ltd.
Manufacturer Address : 207 Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do
57
PharmaCompass offers a list of Latanoprostene Bunod API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Latanoprostene Bunod manufacturer or Latanoprostene Bunod supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Latanoprostene Bunod manufacturer or Latanoprostene Bunod supplier.
A Vyzulta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vyzulta, including repackagers and relabelers. The FDA regulates Vyzulta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vyzulta API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Vyzulta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Vyzulta supplier is an individual or a company that provides Vyzulta active pharmaceutical ingredient (API) or Vyzulta finished formulations upon request. The Vyzulta suppliers may include Vyzulta API manufacturers, exporters, distributors and traders.
click here to find a list of Vyzulta suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Vyzulta Drug Master File in Korea (Vyzulta KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Vyzulta. The MFDS reviews the Vyzulta KDMF as part of the drug registration process and uses the information provided in the Vyzulta KDMF to evaluate the safety and efficacy of the drug.
After submitting a Vyzulta KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Vyzulta API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Vyzulta suppliers with KDMF on PharmaCompass.
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