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Looking for 106635-80-7 / Tafenoquine API manufacturers, exporters & distributors?

Tafenoquine manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Tafenoquine 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 Tafenoquine manufacturer or Tafenoquine supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tafenoquine manufacturer or Tafenoquine supplier.

PharmaCompass also assists you with knowing the Tafenoquine API Price utilized in the formulation of products. Tafenoquine API Price is not always fixed or binding as the Tafenoquine Price is obtained through a variety of data sources. The Tafenoquine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Tafenoquine

Synonyms

106635-80-7, Etaquine, Arakoda, Krintafel, Wr 238605, Sb-252263-aab

Cas Number

106635-80-7

Unique Ingredient Identifier (UNII)

262P8GS9L9

About Tafenoquine

Tafenoquine is an orally bioavailable 8-aminoquinoline derivative, with antimalarial activity. Although the mechanism is not completely understood, upon administration, tafenoquine inhibits the parasitic enzyme heme polymerase in the blood stages of the parasites. This inhibits the conversion of the toxic heme into non-toxic hemazoin, thereby resulting in the accumulation of toxic heme within the parasite. Tafenoquine is active against all the stages of Plasmodium species and is also active against the pre-erythrocytic liver stages of the parasites. This prevents the development of the erythrocytic forms of the parasite which are responsible for relapses in P. vivax malaria.

Tafenoquine Manufacturers

A Tafenoquine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tafenoquine, including repackagers and relabelers. The FDA regulates Tafenoquine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tafenoquine 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 Tafenoquine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Tafenoquine Suppliers

A Tafenoquine supplier is an individual or a company that provides Tafenoquine active pharmaceutical ingredient (API) or Tafenoquine finished formulations upon request. The Tafenoquine suppliers may include Tafenoquine API manufacturers, exporters, distributors and traders.

click here to find a list of Tafenoquine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Tafenoquine NDC

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 Tafenoquine as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Tafenoquine API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 Tafenoquine 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Tafenoquine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tafenoquine NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Tafenoquine suppliers with NDC on PharmaCompass.

Tafenoquine GMP

Tafenoquine 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 Tafenoquine 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 Tafenoquine GMP manufacturer or Tafenoquine GMP API supplier for your needs.

Tafenoquine CoA

A Tafenoquine CoA (Certificate of Analysis) is a formal document that attests to Tafenoquine's compliance with Tafenoquine specifications and serves as a tool for batch-level quality control.

Tafenoquine CoA mostly includes findings from lab analyses of a specific batch. For each Tafenoquine 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.

Tafenoquine may be tested according to a variety of international standards, such as European Pharmacopoeia (Tafenoquine EP), Tafenoquine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tafenoquine USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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