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PharmaCompass offers a list of Foscarnet Sodium 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 Foscarnet Sodium manufacturer or Foscarnet Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Foscarnet Sodium manufacturer or Foscarnet Sodium supplier.
PharmaCompass also assists you with knowing the Foscarnet Sodium API Price utilized in the formulation of products. Foscarnet Sodium API Price is not always fixed or binding as the Foscarnet Sodium Price is obtained through a variety of data sources. The Foscarnet Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Foscarnet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Foscarnet, including repackagers and relabelers. The FDA regulates Foscarnet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Foscarnet 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 Foscarnet manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Foscarnet supplier is an individual or a company that provides Foscarnet active pharmaceutical ingredient (API) or Foscarnet finished formulations upon request. The Foscarnet suppliers may include Foscarnet API manufacturers, exporters, distributors and traders.
click here to find a list of Foscarnet suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Foscarnet DMF (Drug Master File) is a document detailing the whole manufacturing process of Foscarnet active pharmaceutical ingredient (API) in detail. Different forms of Foscarnet DMFs exist exist since differing nations have different regulations, such as Foscarnet USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Foscarnet DMF submitted to regulatory agencies in the US is known as a USDMF. Foscarnet USDMF includes data on Foscarnet's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Foscarnet USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Foscarnet suppliers with USDMF on PharmaCompass.
A Foscarnet CEP of the European Pharmacopoeia monograph is often referred to as a Foscarnet Certificate of Suitability (COS). The purpose of a Foscarnet CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Foscarnet EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Foscarnet to their clients by showing that a Foscarnet CEP has been issued for it. The manufacturer submits a Foscarnet CEP (COS) as part of the market authorization procedure, and it takes on the role of a Foscarnet CEP holder for the record. Additionally, the data presented in the Foscarnet CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Foscarnet DMF.
A Foscarnet CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Foscarnet 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 Foscarnet suppliers with CEP (COS) on PharmaCompass.
A Foscarnet written confirmation (Foscarnet WC) is an official document issued by a regulatory agency to a Foscarnet manufacturer, verifying that the manufacturing facility of a Foscarnet active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Foscarnet APIs or Foscarnet finished pharmaceutical products to another nation, regulatory agencies frequently require a Foscarnet WC (written confirmation) as part of the regulatory process.
click here to find a list of Foscarnet suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Foscarnet as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Foscarnet API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Foscarnet as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Foscarnet and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Foscarnet NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Foscarnet suppliers with NDC on PharmaCompass.
Foscarnet 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 Foscarnet 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 Foscarnet GMP manufacturer or Foscarnet GMP API supplier for your needs.
A Foscarnet CoA (Certificate of Analysis) is a formal document that attests to Foscarnet's compliance with Foscarnet specifications and serves as a tool for batch-level quality control.
Foscarnet CoA mostly includes findings from lab analyses of a specific batch. For each Foscarnet 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.
Foscarnet may be tested according to a variety of international standards, such as European Pharmacopoeia (Foscarnet EP), Foscarnet JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Foscarnet USP).