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01 3EUROAPI FRANCE
02 1Pfizer Inc.
03 1Curia Spain S. A. U.
04 1Henan Lihua Pharmaceutical Co. , Ltd.
01 4Hydrocortisone
02 1Hydrocortisone Sodium Phosphate
03 1Hydrocortisone phosphate ester sodium
01 1China
02 3France
03 2U.S.A
Hydrocortisone sodium phosphate
Registration Number : 220MF10093
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2008-03-28
Latest Date of Registration : 2022-06-22
Registration Number : 222MF10138
Registrant's Address : 235 East 42nd Street, New York, NY 10017
Initial Date of Registration : 2010-04-14
Latest Date of Registration : 2023-03-23
Registration Number : 218MF10377
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2006-03-20
Latest Date of Registration : 2019-11-27
Registration Number : 228MF10090
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2016-04-15
Latest Date of Registration : 2021-03-05
Hydrocortisone Sodium Phosphate
Registration Number : 217MF10680
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2015-09-03
Registration Number : 226MF10036
Registrant's Address : Middle of Huanghe Street, Anyang Hi-Tech Industry Development Zone, Henan, China
Initial Date of Registration : 2014-02-05
Latest Date of Registration : 2017-08-08
A Hydrocortisone Sodium Phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocortisone Sodium Phosphate, including repackagers and relabelers. The FDA regulates Hydrocortisone Sodium Phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocortisone Sodium Phosphate 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 Hydrocortisone Sodium Phosphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrocortisone Sodium Phosphate supplier is an individual or a company that provides Hydrocortisone Sodium Phosphate active pharmaceutical ingredient (API) or Hydrocortisone Sodium Phosphate finished formulations upon request. The Hydrocortisone Sodium Phosphate suppliers may include Hydrocortisone Sodium Phosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrocortisone Sodium Phosphate 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 Hydrocortisone Sodium Phosphate Drug Master File in Japan (Hydrocortisone Sodium Phosphate JDMF) empowers Hydrocortisone Sodium Phosphate 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 Hydrocortisone Sodium Phosphate JDMF during the approval evaluation for pharmaceutical products. At the time of Hydrocortisone Sodium Phosphate 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 Hydrocortisone Sodium Phosphate suppliers with JDMF on PharmaCompass.
We have 4 companies offering Hydrocortisone Sodium Phosphate
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