EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI FRANCE
02 1Curia Spain S. A. U.
03 1Newchem S. p. A.
04 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 2Fluorometholone
02 1Fluorometholone "Teva"
03 1Fluorometholone micronized
01 1France
02 2Italy
03 1U.S.A
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 218MF10387
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2006-03-20
Latest Date of Registration : 2016-12-20
Registration Number : 306MF10063
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2024-05-08
Latest Date of Registration : 2024-05-08
Registration Number : 303MF10110
Registrant's Address : Via de Amicis 47, 20123 Milano, Italy
Initial Date of Registration : 2021-07-16
Latest Date of Registration : 2021-07-16
Registration Number : 218MF10820
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2006-10-06
Latest Date of Registration : 2006-10-06
A Fluorometholone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluorometholone, including repackagers and relabelers. The FDA regulates Fluorometholone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluorometholone 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 Fluorometholone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluorometholone supplier is an individual or a company that provides Fluorometholone active pharmaceutical ingredient (API) or Fluorometholone finished formulations upon request. The Fluorometholone suppliers may include Fluorometholone API manufacturers, exporters, distributors and traders.
click here to find a list of Fluorometholone 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 Fluorometholone Drug Master File in Japan (Fluorometholone JDMF) empowers Fluorometholone 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 Fluorometholone JDMF during the approval evaluation for pharmaceutical products. At the time of Fluorometholone 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 Fluorometholone suppliers with JDMF on PharmaCompass.
We have 4 companies offering Fluorometholone
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