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