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01 EDMOND PHARMA S.R.L. Paderno Dugnano IT (1)
01 Terfenadine (1)
01 Italy (1)
01 Expired (1)
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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 Prestwick3_000138 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000138, including repackagers and relabelers. The FDA regulates Prestwick3_000138 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000138 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 Prestwick3_000138 supplier is an individual or a company that provides Prestwick3_000138 active pharmaceutical ingredient (API) or Prestwick3_000138 finished formulations upon request. The Prestwick3_000138 suppliers may include Prestwick3_000138 API manufacturers, exporters, distributors and traders.
click here to find a list of Prestwick3_000138 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Prestwick3_000138 CEP of the European Pharmacopoeia monograph is often referred to as a Prestwick3_000138 Certificate of Suitability (COS). The purpose of a Prestwick3_000138 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prestwick3_000138 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prestwick3_000138 to their clients by showing that a Prestwick3_000138 CEP has been issued for it. The manufacturer submits a Prestwick3_000138 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prestwick3_000138 CEP holder for the record. Additionally, the data presented in the Prestwick3_000138 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prestwick3_000138 DMF.
A Prestwick3_000138 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prestwick3_000138 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 Prestwick3_000138 suppliers with CEP (COS) on PharmaCompass.
We have 1 companies offering Prestwick3_000138
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