01 1Uquifa Italia S.p.A. Agrate Brianza IT
01 1Carisoprodol - Monograph Text deleted 01/07/2020
01 1Spain
01 1Expired
Carisoprodol - Monograph Text Deleted 01/07/2020
Certificate Number : R0-CEP 2004-128 - Rev 00
Status : Expired
Issue Date : 2008-05-14
Type : Chemical
Substance Number : 1689
16
PharmaCompass offers a list of Carisoprodol 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 Carisoprodol manufacturer or Carisoprodol supplier for your needs.
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PharmaCompass also assists you with knowing the Carisoprodol API Price utilized in the formulation of products. Carisoprodol API Price is not always fixed or binding as the Carisoprodol Price is obtained through a variety of data sources. The Carisoprodol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Isomeprobamate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Isomeprobamate, including repackagers and relabelers. The FDA regulates Isomeprobamate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Isomeprobamate 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 Isomeprobamate supplier is an individual or a company that provides Isomeprobamate active pharmaceutical ingredient (API) or Isomeprobamate finished formulations upon request. The Isomeprobamate suppliers may include Isomeprobamate API manufacturers, exporters, distributors and traders.
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A Isomeprobamate CEP of the European Pharmacopoeia monograph is often referred to as a Isomeprobamate Certificate of Suitability (COS). The purpose of a Isomeprobamate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Isomeprobamate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Isomeprobamate to their clients by showing that a Isomeprobamate CEP has been issued for it. The manufacturer submits a Isomeprobamate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Isomeprobamate CEP holder for the record. Additionally, the data presented in the Isomeprobamate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Isomeprobamate DMF.
A Isomeprobamate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Isomeprobamate 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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