01 1CURIA FRANCE S.A.S. Bon-Encontre FR
02 1Dishman Pharmaceuticals and Chemicals Limited Ahmedabad IN
01 2Hexetidine
01 1India
02 1U.S.A
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2005-238 - Rev 03
Status : Valid
Issue Date : 2022-08-25
Type : Chemical
Substance Number : 1221
Certificate Number : R0-CEP 2010-238 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2012-09-10
Type : Chemical
Substance Number : 1221
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PharmaCompass offers a list of Hexetidine 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 Hexetidine manufacturer or Hexetidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hexetidine manufacturer or Hexetidine supplier.
PharmaCompass also assists you with knowing the Hexetidine API Price utilized in the formulation of products. Hexetidine API Price is not always fixed or binding as the Hexetidine Price is obtained through a variety of data sources. The Hexetidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hexetidinum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexetidinum, including repackagers and relabelers. The FDA regulates Hexetidinum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexetidinum 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 Hexetidinum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hexetidinum supplier is an individual or a company that provides Hexetidinum active pharmaceutical ingredient (API) or Hexetidinum finished formulations upon request. The Hexetidinum suppliers may include Hexetidinum API manufacturers, exporters, distributors and traders.
click here to find a list of Hexetidinum suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hexetidinum CEP of the European Pharmacopoeia monograph is often referred to as a Hexetidinum Certificate of Suitability (COS). The purpose of a Hexetidinum CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hexetidinum EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hexetidinum to their clients by showing that a Hexetidinum CEP has been issued for it. The manufacturer submits a Hexetidinum CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hexetidinum CEP holder for the record. Additionally, the data presented in the Hexetidinum CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hexetidinum DMF.
A Hexetidinum CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hexetidinum 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 Hexetidinum suppliers with CEP (COS) on PharmaCompass.
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