01 1OLON S.P.A. Rodano IT
01 1Mefloquine hydrochloride
01 1Italy
01 1Valid
Certificate Number : CEP 2011-099 - Rev 05
Status : Valid
Issue Date : 2025-02-28
Type : Chemical
Substance Number : 1241
77
PharmaCompass offers a list of Mefloquine 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 Mefloquine manufacturer or Mefloquine supplier for your needs.
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PharmaCompass also assists you with knowing the Mefloquine API Price utilized in the formulation of products. Mefloquine API Price is not always fixed or binding as the Mefloquine Price is obtained through a variety of data sources. The Mefloquine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A WR177,602 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of WR177,602, including repackagers and relabelers. The FDA regulates WR177,602 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. WR177,602 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 WR177,602 supplier is an individual or a company that provides WR177,602 active pharmaceutical ingredient (API) or WR177,602 finished formulations upon request. The WR177,602 suppliers may include WR177,602 API manufacturers, exporters, distributors and traders.
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A WR177,602 CEP of the European Pharmacopoeia monograph is often referred to as a WR177,602 Certificate of Suitability (COS). The purpose of a WR177,602 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of WR177,602 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of WR177,602 to their clients by showing that a WR177,602 CEP has been issued for it. The manufacturer submits a WR177,602 CEP (COS) as part of the market authorization procedure, and it takes on the role of a WR177,602 CEP holder for the record. Additionally, the data presented in the WR177,602 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the WR177,602 DMF.
A WR177,602 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. WR177,602 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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