Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
01 1Cayman Pharma s.r.o
02 1Chirogate International
03 1EUROAPI
04 1Pfizer CentreOne
05 1Guangzhou Tosun Pharmaceutical
06 1Yonsung Fine Chemicals
07 1Zhejiang Ausun Pharmaceutical
Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
About the Company : Cayman Pharma is a leading European provider of cGMP prostaglandin APIs, created in 2006 from the merger of Cayman Chemical and NeraPharm, combining deep prostaglandin chemistry ex...
Chirogate is a professional Prostaglandin manufacturer.
About the Company : Chirogate, established in 1999, is a leading supplier of niche-market molecules, specializing in prostaglandins. Focused on quality and compliance, it offers competitively priced p...
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
About the Company : EUROAPI focuses on reinventing active ingredient solutions to sustainably meet the needs of customers and patients worldwide. The company is a leading API player with a portfolio o...
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
About the Company : Pfizer CentreOne® is an altogether different global contract development and manufacturing organization (CDMO), and a leading supplier of specialty APIs and intermediates.
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PharmaCompass offers a list of Epoprostenol Sodium 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 Epoprostenol Sodium manufacturer or Epoprostenol Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Epoprostenol Sodium API Price utilized in the formulation of products. Epoprostenol Sodium API Price is not always fixed or binding as the Epoprostenol Sodium Price is obtained through a variety of data sources. The Epoprostenol Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A VELETRI manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of VELETRI, including repackagers and relabelers. The FDA regulates VELETRI manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. VELETRI 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 VELETRI supplier is an individual or a company that provides VELETRI active pharmaceutical ingredient (API) or VELETRI finished formulations upon request. The VELETRI suppliers may include VELETRI API manufacturers, exporters, distributors and traders.
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