EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 2EUROAPI Hungary Ltd.
02 1Kanto Chemical Co., Ltd.
03 1YS Life Science Co. , Ltd.
01 2Limaprost Alfadex
02 2Limaprost alfadex
01 2France
02 1Japan
03 1South Korea
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 304MF10134
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2022-09-21
Latest Date of Registration : 2022-09-21
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 219MF10023
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2007-01-22
Latest Date of Registration : 2012-10-03
Registration Number : 218MF10300
Registrant's Address : 3-2-8 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2016-02-18
Registration Number : 222MF10166
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do, 18581, Republic of Korea
Initial Date of Registration : 2010-06-04
Latest Date of Registration : 2010-06-04
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PharmaCompass offers a list of Limaprost Alfadex 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 Limaprost Alfadex manufacturer or Limaprost Alfadex supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Limaprost Alfadex manufacturer or Limaprost Alfadex supplier.
PharmaCompass also assists you with knowing the Limaprost Alfadex API Price utilized in the formulation of products. Limaprost Alfadex API Price is not always fixed or binding as the Limaprost Alfadex Price is obtained through a variety of data sources. The Limaprost Alfadex Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Opalmon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Opalmon, including repackagers and relabelers. The FDA regulates Opalmon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Opalmon 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 Opalmon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Opalmon supplier is an individual or a company that provides Opalmon active pharmaceutical ingredient (API) or Opalmon finished formulations upon request. The Opalmon suppliers may include Opalmon API manufacturers, exporters, distributors and traders.
click here to find a list of Opalmon 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 Opalmon Drug Master File in Japan (Opalmon JDMF) empowers Opalmon 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 Opalmon JDMF during the approval evaluation for pharmaceutical products. At the time of Opalmon 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 Opalmon suppliers with JDMF on PharmaCompass.
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