Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
01 1PHARMACIA & UPJOHN COMPANY LLC Kalamazoo US
02 2EUROAPI FRANCE Vertolaye FR
03 1CURIA SPAIN S.A.U. Boecillo ES
04 3Pharmacia & Upjohn Company Kalamazoo US
05 3TIANJIN TIANYAO PHARMACEUTICALS CO., LTD. Tianjin CN
06 1ZHEJIANG XIANJU JUNYE PHARMACEUTICAL CO., LTD. Xianju CN
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
Certificate Number : R1-CEP 2000-261 - Rev 05
Status : Valid
Issue Date : 2022-09-02
Type : Chemical
Substance Number : 388
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : CEP 1996-019 - Rev 09
Status : Valid
Issue Date : 2024-04-12
Type : Chemical
Substance Number : 388
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : CEP 1998-089 - Rev 08
Status : Valid
Issue Date : 2025-01-22
Type : Chemical
Substance Number : 548
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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.
A MK 125 CEP of the European Pharmacopoeia monograph is often referred to as a MK 125 Certificate of Suitability (COS). The purpose of a MK 125 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MK 125 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MK 125 to their clients by showing that a MK 125 CEP has been issued for it. The manufacturer submits a MK 125 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MK 125 CEP holder for the record. Additionally, the data presented in the MK 125 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MK 125 DMF.
A MK 125 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MK 125 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of MK 125 suppliers with CEP (COS) on PharmaCompass.
We have 6 companies offering MK 125
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