01 1Kongo Chemical Co., Ltd Toyama City JP
01 1Dexchlorpheniramine maleate
01 1Japan
01 1Valid
Certificate Number : R1-CEP 2014-124 - Rev 00
Status : Valid
Issue Date : 2020-09-04
Type : Chemical
Substance Number : 1196
86
PharmaCompass offers a list of Dexchloropheniramine Maleate 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 Dexchloropheniramine Maleate manufacturer or Dexchloropheniramine Maleate supplier for your needs.
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PharmaCompass also assists you with knowing the Dexchloropheniramine Maleate API Price utilized in the formulation of products. Dexchloropheniramine Maleate API Price is not always fixed or binding as the Dexchloropheniramine Maleate Price is obtained through a variety of data sources. The Dexchloropheniramine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dexchloropheniramine Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexchloropheniramine Maleate, including repackagers and relabelers. The FDA regulates Dexchloropheniramine Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexchloropheniramine Maleate 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 Dexchloropheniramine Maleate supplier is an individual or a company that provides Dexchloropheniramine Maleate active pharmaceutical ingredient (API) or Dexchloropheniramine Maleate finished formulations upon request. The Dexchloropheniramine Maleate suppliers may include Dexchloropheniramine Maleate API manufacturers, exporters, distributors and traders.
click here to find a list of Dexchloropheniramine Maleate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dexchloropheniramine Maleate CEP of the European Pharmacopoeia monograph is often referred to as a Dexchloropheniramine Maleate Certificate of Suitability (COS). The purpose of a Dexchloropheniramine Maleate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dexchloropheniramine Maleate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dexchloropheniramine Maleate to their clients by showing that a Dexchloropheniramine Maleate CEP has been issued for it. The manufacturer submits a Dexchloropheniramine Maleate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dexchloropheniramine Maleate CEP holder for the record. Additionally, the data presented in the Dexchloropheniramine Maleate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dexchloropheniramine Maleate DMF.
A Dexchloropheniramine Maleate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dexchloropheniramine Maleate 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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