TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
02 1EXCELLA GMBH & CO. KG Feucht DE
01 1Deferoxamine mesilate, Produced by a synthetic process
02 1Deferoxamine mesilate, Produced by fermentation
01 1Gabon
02 1Israel
01 2Valid
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Deferoxamine Mesilate, Produced By Fermentation
Certificate Number : R1-CEP 2000-160 - Rev 04
Status : Valid
Issue Date : 2022-06-17
Type : Chemical
Substance Number : 896
Deferoxamine Mesilate, Produced By A Synthetic P...
Certificate Number : CEP 2009-401 - Rev 06
Status : Valid
Issue Date : 2025-03-11
Type : Chemical
Substance Number : 896
17
PharmaCompass offers a list of Deferoxamine Mesylate 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 Deferoxamine Mesylate manufacturer or Deferoxamine Mesylate supplier for your needs.
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PharmaCompass also assists you with knowing the Deferoxamine Mesylate API Price utilized in the formulation of products. Deferoxamine Mesylate API Price is not always fixed or binding as the Deferoxamine Mesylate Price is obtained through a variety of data sources. The Deferoxamine Mesylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Deferoxamin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deferoxamin, including repackagers and relabelers. The FDA regulates Deferoxamin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deferoxamin 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 Deferoxamin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Deferoxamin supplier is an individual or a company that provides Deferoxamin active pharmaceutical ingredient (API) or Deferoxamin finished formulations upon request. The Deferoxamin suppliers may include Deferoxamin API manufacturers, exporters, distributors and traders.
click here to find a list of Deferoxamin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Deferoxamin CEP of the European Pharmacopoeia monograph is often referred to as a Deferoxamin Certificate of Suitability (COS). The purpose of a Deferoxamin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Deferoxamin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Deferoxamin to their clients by showing that a Deferoxamin CEP has been issued for it. The manufacturer submits a Deferoxamin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Deferoxamin CEP holder for the record. Additionally, the data presented in the Deferoxamin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Deferoxamin DMF.
A Deferoxamin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Deferoxamin 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 Deferoxamin suppliers with CEP (COS) on PharmaCompass.
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