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01 1Uniqema Gouda NL
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01 1Fatty acid sodium soap base, Prisavon® 1983, Prisavon® 9249, Prisavon® 9250, Prisavon® 9251, Prisavon® 9253,
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01 1Spain
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01 1Expired
Fatty Acid Sodium Soap Base, Prisavon® 1983, Pr...
Certificate Number : R0-CEP 2001-100 - Rev 01
Status : Expired
Issue Date : 2005-03-22
Type : TSE
Substance Number :
20
PharmaCompass offers a list of Sodium Butyrate 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 Sodium Butyrate manufacturer or Sodium Butyrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Butyrate manufacturer or Sodium Butyrate supplier.
PharmaCompass also assists you with knowing the Sodium Butyrate API Price utilized in the formulation of products. Sodium Butyrate API Price is not always fixed or binding as the Sodium Butyrate Price is obtained through a variety of data sources. The Sodium Butyrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BUA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BUA, including repackagers and relabelers. The FDA regulates BUA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BUA 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 BUA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A BUA supplier is an individual or a company that provides BUA active pharmaceutical ingredient (API) or BUA finished formulations upon request. The BUA suppliers may include BUA API manufacturers, exporters, distributors and traders.
click here to find a list of BUA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A BUA CEP of the European Pharmacopoeia monograph is often referred to as a BUA Certificate of Suitability (COS). The purpose of a BUA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of BUA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of BUA to their clients by showing that a BUA CEP has been issued for it. The manufacturer submits a BUA CEP (COS) as part of the market authorization procedure, and it takes on the role of a BUA CEP holder for the record. Additionally, the data presented in the BUA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the BUA DMF.
A BUA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. BUA 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 BUA suppliers with CEP (COS) on PharmaCompass.
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