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01 1DSP Chauny FR
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01 1Colestyramine, Powder, grade AP143/1073
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01 1U.S.A
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01 1Valid
Colestyramine, Powder, Grade AP143/1073
Certificate Number : R1-CEP 2013-343 - Rev 00
Status : Valid
Issue Date : 2020-06-02
Type : Chemical
Substance Number : 1775
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PharmaCompass offers a list of Cholestyramine 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 Cholestyramine manufacturer or Cholestyramine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cholestyramine manufacturer or Cholestyramine supplier.
PharmaCompass also assists you with knowing the Cholestyramine API Price utilized in the formulation of products. Cholestyramine API Price is not always fixed or binding as the Cholestyramine Price is obtained through a variety of data sources. The Cholestyramine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A QUESTRAN LIGHT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of QUESTRAN LIGHT, including repackagers and relabelers. The FDA regulates QUESTRAN LIGHT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. QUESTRAN LIGHT API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A QUESTRAN LIGHT supplier is an individual or a company that provides QUESTRAN LIGHT active pharmaceutical ingredient (API) or QUESTRAN LIGHT finished formulations upon request. The QUESTRAN LIGHT suppliers may include QUESTRAN LIGHT API manufacturers, exporters, distributors and traders.
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A QUESTRAN LIGHT CEP of the European Pharmacopoeia monograph is often referred to as a QUESTRAN LIGHT Certificate of Suitability (COS). The purpose of a QUESTRAN LIGHT CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of QUESTRAN LIGHT EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of QUESTRAN LIGHT to their clients by showing that a QUESTRAN LIGHT CEP has been issued for it. The manufacturer submits a QUESTRAN LIGHT CEP (COS) as part of the market authorization procedure, and it takes on the role of a QUESTRAN LIGHT CEP holder for the record. Additionally, the data presented in the QUESTRAN LIGHT CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the QUESTRAN LIGHT DMF.
A QUESTRAN LIGHT CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. QUESTRAN LIGHT CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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