Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
01 1Cayman Pharma s. r. o.
02 1Pharmacia & Upjohn Company LLC
03 1YS Life Science Co. , Ltd.
01 3Epoprostenol sodium
01 1Czech Republic
02 1South Korea
03 1U.S.A
Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
Registration Number : 221MF10112
Registrant's Address : ul. Pra(´)ce 657,277 11 Neratovice, Czech Republic
Initial Date of Registration : 2009-06-10
Latest Date of Registration : 2018-10-26
Registration Number : 218MF10929
Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA
Initial Date of Registration : 2006-11-21
Latest Date of Registration : 2006-11-21
Registration Number : 222MF10209
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do, 18581, Republic of Korea
Initial Date of Registration : 2010-07-29
Latest Date of Registration : 2022-02-24
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Epoprostenol Sodium manufacturer or Epoprostenol Sodium supplier.
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 Flolan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flolan, including repackagers and relabelers. The FDA regulates Flolan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flolan 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 Flolan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flolan supplier is an individual or a company that provides Flolan active pharmaceutical ingredient (API) or Flolan finished formulations upon request. The Flolan suppliers may include Flolan API manufacturers, exporters, distributors and traders.
click here to find a list of Flolan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Flolan Drug Master File in Japan (Flolan JDMF) empowers Flolan API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Flolan JDMF during the approval evaluation for pharmaceutical products. At the time of Flolan JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Flolan suppliers with JDMF on PharmaCompass.
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