01 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 1UMICORE ARGENTINA S.A. Pilar Industrial Park AR
01 2Lomustine
01 1Gabon
02 1Germany
01 2Valid
Certificate Number : R0-CEP 2021-132 - Rev 00
Status : Valid
Issue Date : 2022-11-10
Type : Chemical
Substance Number : 928
Certificate Number : CEP 2009-141 - Rev 03
Status : Valid
Issue Date : 2024-08-16
Type : Chemical
Substance Number : 928
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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.
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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 CCNU;CeeNU manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CCNU;CeeNU, including repackagers and relabelers. The FDA regulates CCNU;CeeNU manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CCNU;CeeNU API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A CCNU;CeeNU supplier is an individual or a company that provides CCNU;CeeNU active pharmaceutical ingredient (API) or CCNU;CeeNU finished formulations upon request. The CCNU;CeeNU suppliers may include CCNU;CeeNU API manufacturers, exporters, distributors and traders.
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A CCNU;CeeNU CEP of the European Pharmacopoeia monograph is often referred to as a CCNU;CeeNU Certificate of Suitability (COS). The purpose of a CCNU;CeeNU CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CCNU;CeeNU EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CCNU;CeeNU to their clients by showing that a CCNU;CeeNU CEP has been issued for it. The manufacturer submits a CCNU;CeeNU CEP (COS) as part of the market authorization procedure, and it takes on the role of a CCNU;CeeNU CEP holder for the record. Additionally, the data presented in the CCNU;CeeNU CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CCNU;CeeNU DMF.
A CCNU;CeeNU CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CCNU;CeeNU CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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