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01 1JANSSEN PHARMACEUTICA NV Beerse BE
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01 1Clazuril for veterinary use
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01 1Belgium
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01 1Expired
Certificate Number : R0-CEP 2004-145 - Rev 00
Status : Expired
Issue Date : 2006-05-15
Type : Chemical
Substance Number : 1714
59
PharmaCompass offers a list of Clazuril 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 Clazuril manufacturer or Clazuril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clazuril manufacturer or Clazuril supplier.
PharmaCompass also assists you with knowing the Clazuril API Price utilized in the formulation of products. Clazuril API Price is not always fixed or binding as the Clazuril Price is obtained through a variety of data sources. The Clazuril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Appertex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Appertex, including repackagers and relabelers. The FDA regulates Appertex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Appertex API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Appertex supplier is an individual or a company that provides Appertex active pharmaceutical ingredient (API) or Appertex finished formulations upon request. The Appertex suppliers may include Appertex API manufacturers, exporters, distributors and traders.
click here to find a list of Appertex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Appertex CEP of the European Pharmacopoeia monograph is often referred to as a Appertex Certificate of Suitability (COS). The purpose of a Appertex CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Appertex EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Appertex to their clients by showing that a Appertex CEP has been issued for it. The manufacturer submits a Appertex CEP (COS) as part of the market authorization procedure, and it takes on the role of a Appertex CEP holder for the record. Additionally, the data presented in the Appertex CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Appertex DMF.
A Appertex CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Appertex 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 Appertex suppliers with CEP (COS) on PharmaCompass.
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