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01 ESTEVE QUIMICA S.A. Barcelona ES (1)
02 FSP GALENA Wroclaw PL (1)
01 Etamsylate (1)
02 Etamsylate, Code 0122-P54 - Code 0122-P57 (1)
01 Poland (1)
02 Spain (1)
01 Valid (2)
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PharmaCompass offers a list of Ethamsylate 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 Ethamsylate manufacturer or Ethamsylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethamsylate manufacturer or Ethamsylate supplier.
PharmaCompass also assists you with knowing the Ethamsylate API Price utilized in the formulation of products. Ethamsylate API Price is not always fixed or binding as the Ethamsylate Price is obtained through a variety of data sources. The Ethamsylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Altodor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Altodor, including repackagers and relabelers. The FDA regulates Altodor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Altodor 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 Altodor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Altodor supplier is an individual or a company that provides Altodor active pharmaceutical ingredient (API) or Altodor finished formulations upon request. The Altodor suppliers may include Altodor API manufacturers, exporters, distributors and traders.
click here to find a list of Altodor suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Altodor CEP of the European Pharmacopoeia monograph is often referred to as a Altodor Certificate of Suitability (COS). The purpose of a Altodor CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Altodor EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Altodor to their clients by showing that a Altodor CEP has been issued for it. The manufacturer submits a Altodor CEP (COS) as part of the market authorization procedure, and it takes on the role of a Altodor CEP holder for the record. Additionally, the data presented in the Altodor CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Altodor DMF.
A Altodor CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Altodor 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 Altodor suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Altodor
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