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PharmaCompass offers a list of Xenon 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 Xenon manufacturer or Xenon supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Xenon manufacturer or Xenon supplier.
PharmaCompass also assists you with knowing the Xenon API Price utilized in the formulation of products. Xenon API Price is not always fixed or binding as the Xenon Price is obtained through a variety of data sources. The Xenon Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Xenon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xenon, including repackagers and relabelers. The FDA regulates Xenon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xenon API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Xenon supplier is an individual or a company that provides Xenon active pharmaceutical ingredient (API) or Xenon finished formulations upon request. The Xenon suppliers may include Xenon API manufacturers, exporters, distributors and traders.
click here to find a list of Xenon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Xenon DMF (Drug Master File) is a document detailing the whole manufacturing process of Xenon active pharmaceutical ingredient (API) in detail. Different forms of Xenon DMFs exist exist since differing nations have different regulations, such as Xenon USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Xenon DMF submitted to regulatory agencies in the US is known as a USDMF. Xenon USDMF includes data on Xenon's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Xenon USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Xenon suppliers with USDMF on PharmaCompass.
Xenon 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 Xenon 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 Xenon GMP manufacturer or Xenon GMP API supplier for your needs.
A Xenon CoA (Certificate of Analysis) is a formal document that attests to Xenon's compliance with Xenon specifications and serves as a tool for batch-level quality control.
Xenon CoA mostly includes findings from lab analyses of a specific batch. For each Xenon 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.
Xenon may be tested according to a variety of international standards, such as European Pharmacopoeia (Xenon EP), Xenon JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Xenon USP).