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PharmaCompass offers a list of Cytosine 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 Cytosine manufacturer or Cytosine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cytosine manufacturer or Cytosine supplier.
PharmaCompass also assists you with knowing the Cytosine API Price utilized in the formulation of products. Cytosine API Price is not always fixed or binding as the Cytosine Price is obtained through a variety of data sources. The Cytosine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cytosine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cytosine, including repackagers and relabelers. The FDA regulates Cytosine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cytosine 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 Cytosine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cytosine supplier is an individual or a company that provides Cytosine active pharmaceutical ingredient (API) or Cytosine finished formulations upon request. The Cytosine suppliers may include Cytosine API manufacturers, exporters, distributors and traders.
click here to find a list of Cytosine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Cytosine Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Cytosine GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Cytosine GMP manufacturer or Cytosine GMP API supplier for your needs.
A Cytosine CoA (Certificate of Analysis) is a formal document that attests to Cytosine's compliance with Cytosine specifications and serves as a tool for batch-level quality control.
Cytosine CoA mostly includes findings from lab analyses of a specific batch. For each Cytosine CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Cytosine may be tested according to a variety of international standards, such as European Pharmacopoeia (Cytosine EP), Cytosine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cytosine USP).