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PharmaCompass offers a list of Desloratadine 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 Desloratadine manufacturer or Desloratadine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desloratadine manufacturer or Desloratadine supplier.
PharmaCompass also assists you with knowing the Desloratadine API Price utilized in the formulation of products. Desloratadine API Price is not always fixed or binding as the Desloratadine Price is obtained through a variety of data sources. The Desloratadine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Desloratadine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desloratadine, including repackagers and relabelers. The FDA regulates Desloratadine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desloratadine 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 Desloratadine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Desloratadine supplier is an individual or a company that provides Desloratadine active pharmaceutical ingredient (API) or Desloratadine finished formulations upon request. The Desloratadine suppliers may include Desloratadine API manufacturers, exporters, distributors and traders.
click here to find a list of Desloratadine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Desloratadine CEP of the European Pharmacopoeia monograph is often referred to as a Desloratadine Certificate of Suitability (COS). The purpose of a Desloratadine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Desloratadine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Desloratadine to their clients by showing that a Desloratadine CEP has been issued for it. The manufacturer submits a Desloratadine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Desloratadine CEP holder for the record. Additionally, the data presented in the Desloratadine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Desloratadine DMF.
A Desloratadine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Desloratadine 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 Desloratadine suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering Desloratadine
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DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
