01 1OLON S.P.A. Rodano IT
01 1Mefloquine hydrochloride
01 1Italy
01 1Valid
Certificate Number : CEP 2011-099 - Rev 04
Status : Valid
Issue Date : 2024-07-11
Type : Chemical
Substance Number : 1241
32
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 (+/-)-Mefloquine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+/-)-Mefloquine Hydrochloride, including repackagers and relabelers. The FDA regulates (+/-)-Mefloquine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+/-)-Mefloquine Hydrochloride 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 (+/-)-Mefloquine Hydrochloride supplier is an individual or a company that provides (+/-)-Mefloquine Hydrochloride active pharmaceutical ingredient (API) or (+/-)-Mefloquine Hydrochloride finished formulations upon request. The (+/-)-Mefloquine Hydrochloride suppliers may include (+/-)-Mefloquine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of (+/-)-Mefloquine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A (+/-)-Mefloquine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a (+/-)-Mefloquine Hydrochloride Certificate of Suitability (COS). The purpose of a (+/-)-Mefloquine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of (+/-)-Mefloquine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of (+/-)-Mefloquine Hydrochloride to their clients by showing that a (+/-)-Mefloquine Hydrochloride CEP has been issued for it. The manufacturer submits a (+/-)-Mefloquine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a (+/-)-Mefloquine Hydrochloride CEP holder for the record. Additionally, the data presented in the (+/-)-Mefloquine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the (+/-)-Mefloquine Hydrochloride DMF.
A (+/-)-Mefloquine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. (+/-)-Mefloquine Hydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of (+/-)-Mefloquine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
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