EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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01 1EUROAPI FRANCE
02 1Curia Spain S. A. U.
03 1Newchem S. p. A.
04 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
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01 2Fluorometholone
02 1Fluorometholone "Teva"
03 1Fluorometholone micronized
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01 1France
02 2Italy
03 1U.S.A
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
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PharmaCompass offers a list of Fluorometholone 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 Fluorometholone manufacturer or Fluorometholone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluorometholone manufacturer or Fluorometholone supplier.
PharmaCompass also assists you with knowing the Fluorometholone API Price utilized in the formulation of products. Fluorometholone API Price is not always fixed or binding as the Fluorometholone Price is obtained through a variety of data sources. The Fluorometholone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A FML Liquifilm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FML Liquifilm, including repackagers and relabelers. The FDA regulates FML Liquifilm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FML Liquifilm 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 FML Liquifilm manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A FML Liquifilm supplier is an individual or a company that provides FML Liquifilm active pharmaceutical ingredient (API) or FML Liquifilm finished formulations upon request. The FML Liquifilm suppliers may include FML Liquifilm API manufacturers, exporters, distributors and traders.
click here to find a list of FML Liquifilm 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 FML Liquifilm Drug Master File in Japan (FML Liquifilm JDMF) empowers FML Liquifilm 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 FML Liquifilm JDMF during the approval evaluation for pharmaceutical products. At the time of FML Liquifilm 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 FML Liquifilm suppliers with JDMF on PharmaCompass.
We have 4 companies offering FML Liquifilm
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