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01 KATWIJK CHEMIE BV Katwijk ZH NL (1)
01 Ethosuximide (1)
01 Netherlands (1)
01 Valid (1)
100
PharmaCompass offers a list of Ethosuximide 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 Ethosuximide manufacturer or Ethosuximide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethosuximide manufacturer or Ethosuximide supplier.
PharmaCompass also assists you with knowing the Ethosuximide API Price utilized in the formulation of products. Ethosuximide API Price is not always fixed or binding as the Ethosuximide Price is obtained through a variety of data sources. The Ethosuximide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ethosuximide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethosuximide, including repackagers and relabelers. The FDA regulates Ethosuximide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethosuximide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Ethosuximide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ethosuximide supplier is an individual or a company that provides Ethosuximide active pharmaceutical ingredient (API) or Ethosuximide finished formulations upon request. The Ethosuximide suppliers may include Ethosuximide API manufacturers, exporters, distributors and traders.
click here to find a list of Ethosuximide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ethosuximide CEP of the European Pharmacopoeia monograph is often referred to as a Ethosuximide Certificate of Suitability (COS). The purpose of a Ethosuximide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ethosuximide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ethosuximide to their clients by showing that a Ethosuximide CEP has been issued for it. The manufacturer submits a Ethosuximide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ethosuximide CEP holder for the record. Additionally, the data presented in the Ethosuximide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ethosuximide DMF.
A Ethosuximide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ethosuximide 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 Ethosuximide suppliers with CEP (COS) on PharmaCompass.
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