Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
01 1Pfizer Inc.
02 1EUROAPI FRANCE
01 1Hydrocortisone Acetate
02 1Hydrocortisone acetate
01 1France
02 1U.S.A
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
Registration Number : 217MF10978
Registrant's Address : 235 East 42nd Street, New York, NY 10017
Initial Date of Registration : 2005-11-14
Latest Date of Registration : 2025-10-29
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 220MF10078
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2008-03-14
Latest Date of Registration : 2019-08-20
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PharmaCompass offers a list of Hydrocortisone Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Hydrocortisone Acetate manufacturer or Hydrocortisone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrocortisone Acetate manufacturer or Hydrocortisone Acetate supplier.
A DRICORT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DRICORT, including repackagers and relabelers. The FDA regulates DRICORT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DRICORT 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 DRICORT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A DRICORT supplier is an individual or a company that provides DRICORT active pharmaceutical ingredient (API) or DRICORT finished formulations upon request. The DRICORT suppliers may include DRICORT API manufacturers, exporters, distributors and traders.
click here to find a list of DRICORT suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 DRICORT Drug Master File in Japan (DRICORT JDMF) empowers DRICORT 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 DRICORT JDMF during the approval evaluation for pharmaceutical products. At the time of DRICORT 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 DRICORT suppliers with JDMF on PharmaCompass.
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