EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 2EUROAPI FRANCE
02 1STEROID S. p. A.
01 1Dexamethasone meth sulfobenzoic acid ester sodium
02 1Dexamethasone phosphate ester sodium
03 1Japanese Pharmaceutical Codex dexamethasone meth sulfobenzoic acid ester sodium (manufactured only)
01 2France
02 1Italy
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Dexamethasone sodium phosphate
Registration Number : 222MF10092
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2010-03-17
Latest Date of Registration : 2020-09-14
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Dexamethasone metasulfobenzoate sodium
Registration Number : 222MF10093
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2010-03-17
Latest Date of Registration : 2016-03-07
Registration Number : 221MF10245
Registrant's Address : Viale Spagna, 156 Cologno Monzese (MI) - ITALY
Initial Date of Registration : 2009-11-16
Latest Date of Registration : 2009-11-16
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PharmaCompass offers a list of Dexamethasone Sodium Phosphate 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 Sodium Phosphate manufacturer or Dexamethasone Sodium Phosphate supplier for your needs.
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PharmaCompass also assists you with knowing the Dexamethasone Sodium Phosphate API Price utilized in the formulation of products. Dexamethasone Sodium Phosphate API Price is not always fixed or binding as the Dexamethasone Sodium Phosphate Price is obtained through a variety of data sources. The Dexamethasone Sodium Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KS-1150 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KS-1150, including repackagers and relabelers. The FDA regulates KS-1150 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KS-1150 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 KS-1150 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KS-1150 supplier is an individual or a company that provides KS-1150 active pharmaceutical ingredient (API) or KS-1150 finished formulations upon request. The KS-1150 suppliers may include KS-1150 API manufacturers, exporters, distributors and traders.
click here to find a list of KS-1150 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 KS-1150 Drug Master File in Japan (KS-1150 JDMF) empowers KS-1150 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 KS-1150 JDMF during the approval evaluation for pharmaceutical products. At the time of KS-1150 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 KS-1150 suppliers with JDMF on PharmaCompass.
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