EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI FRANCE
02 3Curia Spain S. A. U.
03 1Pharmacia & Upjohn Company LLC
04 1Sicor de Me(´)xico,S. A. de C. V.
01 1Day stations dexamethasone (production only)
02 2Dexamethasone
03 1Dexamethasone Propionate
04 1Dexamethasone valerate
05 1Dexamethasone valerate micronized
01 1France
02 1Mexico
03 4U.S.A
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 218MF10376
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2006-03-20
Latest Date of Registration : 2024-08-22
Dexamethasone valerate micronized
Registration Number : 227MF10063
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2015-03-06
Latest Date of Registration : 2016-11-18
Registration Number : 217MF11173
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2009-12-15
JP Dexamethasone (for manufacturing only)
Registration Number : 218MF10748
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2010-03-17
Registration Number : 221MF10091
Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA
Initial Date of Registration : 2009-05-13
Latest Date of Registration : 2010-05-31
Registration Number : 218MF10901
Registrant's Address : Av. San Rafael No. 35 Parque Industrial Lerma, CP52000 Lerma, Edo. Me(´)xico. MEXICO
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2024-06-06
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PharmaCompass offers a list of Dexamethasone 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 Dexamethasone manufacturer or Dexamethasone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dexamethasone manufacturer or Dexamethasone supplier.
PharmaCompass also assists you with knowing the Dexamethasone API Price utilized in the formulation of products. Dexamethasone API Price is not always fixed or binding as the Dexamethasone Price is obtained through a variety of data sources. The Dexamethasone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MK 125 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MK 125, including repackagers and relabelers. The FDA regulates MK 125 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MK 125 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 MK 125 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MK 125 supplier is an individual or a company that provides MK 125 active pharmaceutical ingredient (API) or MK 125 finished formulations upon request. The MK 125 suppliers may include MK 125 API manufacturers, exporters, distributors and traders.
click here to find a list of MK 125 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 MK 125 Drug Master File in Japan (MK 125 JDMF) empowers MK 125 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 MK 125 JDMF during the approval evaluation for pharmaceutical products. At the time of MK 125 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 MK 125 suppliers with JDMF on PharmaCompass.
We have 4 companies offering MK 125
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