01 1DISHMAN CARBOGEN AMCIS LIMITED Ahmedabad IN
02 1Medichem, S.A. Sant Joan Despí ES
01 2Chlorhexidine dihydrochloride
01 1Spain
02 1Switzerland
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2010-215 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2019-09-17
Type : Chemical
Substance Number : 659
Certificate Number : CEP 2018-081 - Rev 02
Status : Valid
Issue Date : 2024-02-19
Type : Chemical
Substance Number : 659
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PharmaCompass offers a list of Chlorhexidine Hydrochloride 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 Chlorhexidine Hydrochloride manufacturer or Chlorhexidine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorhexidine Hydrochloride manufacturer or Chlorhexidine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Chlorhexidine Hydrochloride API Price utilized in the formulation of products. Chlorhexidine Hydrochloride API Price is not always fixed or binding as the Chlorhexidine Hydrochloride Price is obtained through a variety of data sources. The Chlorhexidine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dantroche hibitane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dantroche hibitane, including repackagers and relabelers. The FDA regulates Dantroche hibitane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dantroche hibitane 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 Dantroche hibitane supplier is an individual or a company that provides Dantroche hibitane active pharmaceutical ingredient (API) or Dantroche hibitane finished formulations upon request. The Dantroche hibitane suppliers may include Dantroche hibitane API manufacturers, exporters, distributors and traders.
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A Dantroche hibitane CEP of the European Pharmacopoeia monograph is often referred to as a Dantroche hibitane Certificate of Suitability (COS). The purpose of a Dantroche hibitane CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dantroche hibitane EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dantroche hibitane to their clients by showing that a Dantroche hibitane CEP has been issued for it. The manufacturer submits a Dantroche hibitane CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dantroche hibitane CEP holder for the record. Additionally, the data presented in the Dantroche hibitane CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dantroche hibitane DMF.
A Dantroche hibitane CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dantroche hibitane 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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