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PharmaCompass offers a list of Artesunate 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 Artesunate manufacturer or Artesunate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Artesunate manufacturer or Artesunate supplier.
PharmaCompass also assists you with knowing the Artesunate API Price utilized in the formulation of products. Artesunate API Price is not always fixed or binding as the Artesunate Price is obtained through a variety of data sources. The Artesunate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Artesunate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Artesunate, including repackagers and relabelers. The FDA regulates Artesunate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Artesunate 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 Artesunate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Artesunate supplier is an individual or a company that provides Artesunate active pharmaceutical ingredient (API) or Artesunate finished formulations upon request. The Artesunate suppliers may include Artesunate API manufacturers, exporters, distributors and traders.
click here to find a list of Artesunate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Artesunate DMF (Drug Master File) is a document detailing the whole manufacturing process of Artesunate active pharmaceutical ingredient (API) in detail. Different forms of Artesunate DMFs exist exist since differing nations have different regulations, such as Artesunate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Artesunate DMF submitted to regulatory agencies in the US is known as a USDMF. Artesunate USDMF includes data on Artesunate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Artesunate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Artesunate suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Artesunate Drug Master File in Korea (Artesunate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Artesunate. The MFDS reviews the Artesunate KDMF as part of the drug registration process and uses the information provided in the Artesunate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Artesunate KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Artesunate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Artesunate suppliers with KDMF on PharmaCompass.
A Artesunate written confirmation (Artesunate WC) is an official document issued by a regulatory agency to a Artesunate manufacturer, verifying that the manufacturing facility of a Artesunate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Artesunate APIs or Artesunate finished pharmaceutical products to another nation, regulatory agencies frequently require a Artesunate WC (written confirmation) as part of the regulatory process.
click here to find a list of Artesunate 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 Artesunate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Artesunate 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 Artesunate 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 Artesunate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Artesunate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Artesunate suppliers with NDC on PharmaCompass.
Artesunate 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 Artesunate 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 Artesunate GMP manufacturer or Artesunate GMP API supplier for your needs.
A Artesunate CoA (Certificate of Analysis) is a formal document that attests to Artesunate's compliance with Artesunate specifications and serves as a tool for batch-level quality control.
Artesunate CoA mostly includes findings from lab analyses of a specific batch. For each Artesunate 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.
Artesunate may be tested according to a variety of international standards, such as European Pharmacopoeia (Artesunate EP), Artesunate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Artesunate USP).
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