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01 1EDMOND PHARMA S.R.L. Paderno Dugnano IT
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01 1Terfenadine
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01 1Italy
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01 1Expired
Certificate Number : R1-CEP 1997-010 - Rev 01
Status : Expired
Issue Date : 2004-10-28
Type : Chemical
Substance Number : 955
62
PharmaCompass offers a list of Terfenadine 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 Terfenadine manufacturer or Terfenadine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Terfenadine manufacturer or Terfenadine supplier.
PharmaCompass also assists you with knowing the Terfenadine API Price utilized in the formulation of products. Terfenadine API Price is not always fixed or binding as the Terfenadine Price is obtained through a variety of data sources. The Terfenadine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rapidal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rapidal, including repackagers and relabelers. The FDA regulates Rapidal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rapidal 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 Rapidal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rapidal supplier is an individual or a company that provides Rapidal active pharmaceutical ingredient (API) or Rapidal finished formulations upon request. The Rapidal suppliers may include Rapidal API manufacturers, exporters, distributors and traders.
click here to find a list of Rapidal suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rapidal CEP of the European Pharmacopoeia monograph is often referred to as a Rapidal Certificate of Suitability (COS). The purpose of a Rapidal CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Rapidal EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Rapidal to their clients by showing that a Rapidal CEP has been issued for it. The manufacturer submits a Rapidal CEP (COS) as part of the market authorization procedure, and it takes on the role of a Rapidal CEP holder for the record. Additionally, the data presented in the Rapidal CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Rapidal DMF.
A Rapidal CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Rapidal 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 Rapidal suppliers with CEP (COS) on PharmaCompass.