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Status : Withdrawn by Holder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 Hexetidina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexetidina, including repackagers and relabelers. The FDA regulates Hexetidina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexetidina 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 Hexetidina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hexetidina supplier is an individual or a company that provides Hexetidina active pharmaceutical ingredient (API) or Hexetidina finished formulations upon request. The Hexetidina suppliers may include Hexetidina API manufacturers, exporters, distributors and traders.
click here to find a list of Hexetidina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hexetidina CEP of the European Pharmacopoeia monograph is often referred to as a Hexetidina Certificate of Suitability (COS). The purpose of a Hexetidina CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hexetidina EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hexetidina to their clients by showing that a Hexetidina CEP has been issued for it. The manufacturer submits a Hexetidina CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hexetidina CEP holder for the record. Additionally, the data presented in the Hexetidina CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hexetidina DMF.
A Hexetidina CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hexetidina 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 Hexetidina suppliers with CEP (COS) on PharmaCompass.
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