LEBSA- Your strategic API source for niche molecules.
01 1Laboratorios Espinos Y Bofill S.A. Cornella de Llobregat ES
01 1Dequalinium chloride
01 1Spain
01 1Valid
LEBSA- Your strategic API source for niche molecules.
LEBSA- Your strategic API source for niche molecules.
Certificate Number : CEP 2019-026 - Rev 03
Status : Valid
Issue Date : 2025-11-26
Type : Chemical
Substance Number : 1413
88
PharmaCompass offers a list of Dequalinium Chloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Dequalinium Chloride manufacturer or Dequalinium Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dequalinium Chloride manufacturer or Dequalinium Chloride supplier.
A Dequalinium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dequalinium, including repackagers and relabelers. The FDA regulates Dequalinium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dequalinium 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 Dequalinium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Dequalinium supplier is an individual or a company that provides Dequalinium active pharmaceutical ingredient (API) or Dequalinium finished formulations upon request. The Dequalinium suppliers may include Dequalinium API manufacturers, exporters, distributors and traders.
click here to find a list of Dequalinium suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Dequalinium CEP of the European Pharmacopoeia monograph is often referred to as a Dequalinium Certificate of Suitability (COS). The purpose of a Dequalinium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dequalinium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dequalinium to their clients by showing that a Dequalinium CEP has been issued for it. The manufacturer submits a Dequalinium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dequalinium CEP holder for the record. Additionally, the data presented in the Dequalinium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dequalinium DMF.
A Dequalinium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dequalinium 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 Dequalinium suppliers with CEP (COS) on PharmaCompass.
