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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 sodico manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Foscarnet sodico, including repackagers and relabelers. The FDA regulates Foscarnet sodico manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Foscarnet sodico 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 sodico manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Foscarnet sodico supplier is an individual or a company that provides Foscarnet sodico active pharmaceutical ingredient (API) or Foscarnet sodico finished formulations upon request. The Foscarnet sodico suppliers may include Foscarnet sodico API manufacturers, exporters, distributors and traders.
click here to find a list of Foscarnet sodico suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Foscarnet sodico DMF (Drug Master File) is a document detailing the whole manufacturing process of Foscarnet sodico active pharmaceutical ingredient (API) in detail. Different forms of Foscarnet sodico DMFs exist exist since differing nations have different regulations, such as Foscarnet sodico USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Foscarnet sodico DMF submitted to regulatory agencies in the US is known as a USDMF. Foscarnet sodico USDMF includes data on Foscarnet sodico's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Foscarnet sodico USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Foscarnet sodico suppliers with USDMF on PharmaCompass.
A Foscarnet sodico CEP of the European Pharmacopoeia monograph is often referred to as a Foscarnet sodico Certificate of Suitability (COS). The purpose of a Foscarnet sodico CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Foscarnet sodico EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Foscarnet sodico to their clients by showing that a Foscarnet sodico CEP has been issued for it. The manufacturer submits a Foscarnet sodico CEP (COS) as part of the market authorization procedure, and it takes on the role of a Foscarnet sodico CEP holder for the record. Additionally, the data presented in the Foscarnet sodico CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Foscarnet sodico DMF.
A Foscarnet sodico CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Foscarnet sodico 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 sodico suppliers with CEP (COS) on PharmaCompass.
A Foscarnet sodico written confirmation (Foscarnet sodico WC) is an official document issued by a regulatory agency to a Foscarnet sodico manufacturer, verifying that the manufacturing facility of a Foscarnet sodico active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Foscarnet sodico APIs or Foscarnet sodico finished pharmaceutical products to another nation, regulatory agencies frequently require a Foscarnet sodico WC (written confirmation) as part of the regulatory process.
click here to find a list of Foscarnet sodico 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 sodico as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Foscarnet sodico 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 sodico 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 sodico and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Foscarnet sodico NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Foscarnet sodico suppliers with NDC on PharmaCompass.
Foscarnet sodico 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 sodico 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 sodico GMP manufacturer or Foscarnet sodico GMP API supplier for your needs.
A Foscarnet sodico CoA (Certificate of Analysis) is a formal document that attests to Foscarnet sodico's compliance with Foscarnet sodico specifications and serves as a tool for batch-level quality control.
Foscarnet sodico CoA mostly includes findings from lab analyses of a specific batch. For each Foscarnet sodico 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 sodico may be tested according to a variety of international standards, such as European Pharmacopoeia (Foscarnet sodico EP), Foscarnet sodico JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Foscarnet sodico USP).
