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