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 Dexclor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexclor, including repackagers and relabelers. The FDA regulates Dexclor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexclor 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 Dexclor supplier is an individual or a company that provides Dexclor active pharmaceutical ingredient (API) or Dexclor finished formulations upon request. The Dexclor suppliers may include Dexclor API manufacturers, exporters, distributors and traders.
click here to find a list of Dexclor suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dexclor CEP of the European Pharmacopoeia monograph is often referred to as a Dexclor Certificate of Suitability (COS). The purpose of a Dexclor CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dexclor EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dexclor to their clients by showing that a Dexclor CEP has been issued for it. The manufacturer submits a Dexclor CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dexclor CEP holder for the record. Additionally, the data presented in the Dexclor CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dexclor DMF.
A Dexclor CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dexclor 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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