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