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Status : Withdrawn by Holder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
18
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 38805A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 38805A, including repackagers and relabelers. The FDA regulates 38805A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 38805A 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 38805A manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 38805A supplier is an individual or a company that provides 38805A active pharmaceutical ingredient (API) or 38805A finished formulations upon request. The 38805A suppliers may include 38805A API manufacturers, exporters, distributors and traders.
click here to find a list of 38805A suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 38805A CEP of the European Pharmacopoeia monograph is often referred to as a 38805A Certificate of Suitability (COS). The purpose of a 38805A CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 38805A EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 38805A to their clients by showing that a 38805A CEP has been issued for it. The manufacturer submits a 38805A CEP (COS) as part of the market authorization procedure, and it takes on the role of a 38805A CEP holder for the record. Additionally, the data presented in the 38805A CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 38805A DMF.
A 38805A CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 38805A 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 38805A suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering 38805A
Get in contact with the supplier of your choice:
