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
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
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
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
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
A Dexamethasone Dipropionate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexamethasone Dipropionate, including repackagers and relabelers. The FDA regulates Dexamethasone Dipropionate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexamethasone Dipropionate 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 Dexamethasone Dipropionate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dexamethasone Dipropionate supplier is an individual or a company that provides Dexamethasone Dipropionate active pharmaceutical ingredient (API) or Dexamethasone Dipropionate finished formulations upon request. The Dexamethasone Dipropionate suppliers may include Dexamethasone Dipropionate API manufacturers, exporters, distributors and traders.
click here to find a list of Dexamethasone Dipropionate 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 Dexamethasone Dipropionate Drug Master File in Japan (Dexamethasone Dipropionate JDMF) empowers Dexamethasone Dipropionate 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 Dexamethasone Dipropionate JDMF during the approval evaluation for pharmaceutical products. At the time of Dexamethasone Dipropionate 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 Dexamethasone Dipropionate suppliers with JDMF on PharmaCompass.
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