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PharmaCompass offers a list of Capecitabine 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 Capecitabine manufacturer or Capecitabine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Capecitabine manufacturer or Capecitabine supplier.
PharmaCompass also assists you with knowing the Capecitabine API Price utilized in the formulation of products. Capecitabine API Price is not always fixed or binding as the Capecitabine Price is obtained through a variety of data sources. The Capecitabine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Capecitabine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Capecitabine, including repackagers and relabelers. The FDA regulates Capecitabine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Capecitabine 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 Capecitabine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Capecitabine supplier is an individual or a company that provides Capecitabine active pharmaceutical ingredient (API) or Capecitabine finished formulations upon request. The Capecitabine suppliers may include Capecitabine API manufacturers, exporters, distributors and traders.
click here to find a list of Capecitabine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Capecitabine CEP of the European Pharmacopoeia monograph is often referred to as a Capecitabine Certificate of Suitability (COS). The purpose of a Capecitabine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Capecitabine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Capecitabine to their clients by showing that a Capecitabine CEP has been issued for it. The manufacturer submits a Capecitabine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Capecitabine CEP holder for the record. Additionally, the data presented in the Capecitabine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Capecitabine DMF.
A Capecitabine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Capecitabine 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 Capecitabine suppliers with CEP (COS) on PharmaCompass.
We have 18 companies offering Capecitabine
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DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
