Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
01 1PHARMACIA & UPJOHN COMPANY LLC Kalamazoo US
02 1EUROAPI FRANCE Vertolaye FR
03 1CURIA SPAIN S.A.U. Boecillo ES
04 1SM BIOMED SDN BHD Sungai Petani MY
05 1SYMBIOTICA SPECIALITY INGREDIENTS SDN. BHD. Perai MY
06 1TIANJIN TIANYAO PHARMACEUTICALS CO., LTD. Tianjin CN
07 1XI’AN GUOKANG RUIJIN PHARMACEUTICAL CO., LTD. Xi’an City CN
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
Dexamethasone Sodium Phosphate
Certificate Number : R1-CEP 1998-154 - Rev 06
Status : Valid
Issue Date : 2021-07-07
Type : Chemical
Substance Number : 549
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Dexamethasone Sodium Phosphate
Certificate Number : R2-CEP 1992-014 - Rev 07
Status : Valid
Issue Date : 2021-12-16
Type : Chemical
Substance Number : 549
98
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 Hexadrol Injectable manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexadrol Injectable, including repackagers and relabelers. The FDA regulates Hexadrol Injectable manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexadrol Injectable 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 Hexadrol Injectable manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hexadrol Injectable supplier is an individual or a company that provides Hexadrol Injectable active pharmaceutical ingredient (API) or Hexadrol Injectable finished formulations upon request. The Hexadrol Injectable suppliers may include Hexadrol Injectable API manufacturers, exporters, distributors and traders.
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A Hexadrol Injectable CEP of the European Pharmacopoeia monograph is often referred to as a Hexadrol Injectable Certificate of Suitability (COS). The purpose of a Hexadrol Injectable CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hexadrol Injectable EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hexadrol Injectable to their clients by showing that a Hexadrol Injectable CEP has been issued for it. The manufacturer submits a Hexadrol Injectable CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hexadrol Injectable CEP holder for the record. Additionally, the data presented in the Hexadrol Injectable CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hexadrol Injectable DMF.
A Hexadrol Injectable CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hexadrol Injectable 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 Hexadrol Injectable suppliers with CEP (COS) on PharmaCompass.
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