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