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