EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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01 1EUROAPI Hungary Ltd.
02 1YS Life Science Co. , Ltd.
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01 2Alprostadil
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01 1France
02 1South Korea
Registration Number : 220MF10064
Registrant's Address : To (´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2008-02-25
Latest Date of Registration : 2025-11-05
Registration Number : 306MF10135
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Manse-gu, Hwaseong-si, Gyeonggi-do, 18581, Republic of...
Initial Date of Registration : 2024-10-16
Latest Date of Registration : 2025-09-03

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PharmaCompass offers a list of Alprostadil 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 Alprostadil manufacturer or Alprostadil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Alprostadil manufacturer or Alprostadil supplier.
PharmaCompass also assists you with knowing the Alprostadil API Price utilized in the formulation of products. Alprostadil API Price is not always fixed or binding as the Alprostadil Price is obtained through a variety of data sources. The Alprostadil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Femprox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Femprox, including repackagers and relabelers. The FDA regulates Femprox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Femprox 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 Femprox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Femprox supplier is an individual or a company that provides Femprox active pharmaceutical ingredient (API) or Femprox finished formulations upon request. The Femprox suppliers may include Femprox API manufacturers, exporters, distributors and traders.
click here to find a list of Femprox 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 Femprox Drug Master File in Japan (Femprox JDMF) empowers Femprox 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 Femprox JDMF during the approval evaluation for pharmaceutical products. At the time of Femprox 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 Femprox suppliers with JDMF on PharmaCompass.
We have 2 companies offering Femprox
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