Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
01 1Cayman Pharma sro
02 1(주)와이에스생명과학
03 1MSN Laboratories Private Limited
01 1(주)와이에스생명과학
02 1Klasia Co., Ltd.
03 1엠피크코리아(주)
01 3Latanoprostene Bunod
01 1Czech Republic
02 1India
03 1South Korea
Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
Registrant Name : Klasia Co., Ltd.
Registration Date : 2024-01-15
Registration Number : No. 758-10-ND
Manufacturer Name : Cayman Pharma sro
Manufacturer Address : Práce 657, 277 11 Neratovice, Czech Republic
Registrant Name : 엠피크코리아(주)
Registration Date : 2025-02-28
Registration Number : Number 812-25-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 : (주)와이에스생명과학
Registration Date : 2024-10-09
Registration Number : 2247-1-ND
Manufacturer Name : (주)와이에스생명과...
Manufacturer Address : 경기도 화성시 장안면 수정로 207
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PharmaCompass offers a list of Latanoprostene Bunod API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Latanoprostene Bunod manufacturer or Latanoprostene Bunod supplier for your needs.
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PharmaCompass also assists you with knowing the Latanoprostene Bunod API Price utilized in the formulation of products. Latanoprostene Bunod API Price is not always fixed or binding as the Latanoprostene Bunod Price is obtained through a variety of data sources. The Latanoprostene Bunod Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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.
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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, COA and API Price 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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