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