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Looking for 17902-23-7 / Tegafur API manufacturers, exporters & distributors?

Tegafur manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Tegafur

Synonyms

Ftorafur, 17902-23-7, Futraful, Sinoflurol, Fental, Fluorofur

Cas Number

17902-23-7

Unique Ingredient Identifier (UNII)

1548R74NSZ

About Tegafur

Congener of FLUOROURACIL with comparable antineoplastic action. It has been suggested especially for the treatment of breast neoplasms.

1-(2-Tetrahydrofuryl)-5-fluorouracil Manufacturers

A 1-(2-Tetrahydrofuryl)-5-fluorouracil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1-(2-Tetrahydrofuryl)-5-fluorouracil, including repackagers and relabelers. The FDA regulates 1-(2-Tetrahydrofuryl)-5-fluorouracil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1-(2-Tetrahydrofuryl)-5-fluorouracil 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 1-(2-Tetrahydrofuryl)-5-fluorouracil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

1-(2-Tetrahydrofuryl)-5-fluorouracil Suppliers

A 1-(2-Tetrahydrofuryl)-5-fluorouracil supplier is an individual or a company that provides 1-(2-Tetrahydrofuryl)-5-fluorouracil active pharmaceutical ingredient (API) or 1-(2-Tetrahydrofuryl)-5-fluorouracil finished formulations upon request. The 1-(2-Tetrahydrofuryl)-5-fluorouracil suppliers may include 1-(2-Tetrahydrofuryl)-5-fluorouracil API manufacturers, exporters, distributors and traders.

click here to find a list of 1-(2-Tetrahydrofuryl)-5-fluorouracil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

1-(2-Tetrahydrofuryl)-5-fluorouracil USDMF

A 1-(2-Tetrahydrofuryl)-5-fluorouracil DMF (Drug Master File) is a document detailing the whole manufacturing process of 1-(2-Tetrahydrofuryl)-5-fluorouracil active pharmaceutical ingredient (API) in detail. Different forms of 1-(2-Tetrahydrofuryl)-5-fluorouracil DMFs exist exist since differing nations have different regulations, such as 1-(2-Tetrahydrofuryl)-5-fluorouracil USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 1-(2-Tetrahydrofuryl)-5-fluorouracil DMF submitted to regulatory agencies in the US is known as a USDMF. 1-(2-Tetrahydrofuryl)-5-fluorouracil USDMF includes data on 1-(2-Tetrahydrofuryl)-5-fluorouracil's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1-(2-Tetrahydrofuryl)-5-fluorouracil USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 1-(2-Tetrahydrofuryl)-5-fluorouracil suppliers with USDMF on PharmaCompass.

1-(2-Tetrahydrofuryl)-5-fluorouracil JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The 1-(2-Tetrahydrofuryl)-5-fluorouracil Drug Master File in Japan (1-(2-Tetrahydrofuryl)-5-fluorouracil JDMF) empowers 1-(2-Tetrahydrofuryl)-5-fluorouracil API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the 1-(2-Tetrahydrofuryl)-5-fluorouracil JDMF during the approval evaluation for pharmaceutical products. At the time of 1-(2-Tetrahydrofuryl)-5-fluorouracil JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of 1-(2-Tetrahydrofuryl)-5-fluorouracil suppliers with JDMF on PharmaCompass.

1-(2-Tetrahydrofuryl)-5-fluorouracil KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a 1-(2-Tetrahydrofuryl)-5-fluorouracil Drug Master File in Korea (1-(2-Tetrahydrofuryl)-5-fluorouracil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 1-(2-Tetrahydrofuryl)-5-fluorouracil. The MFDS reviews the 1-(2-Tetrahydrofuryl)-5-fluorouracil KDMF as part of the drug registration process and uses the information provided in the 1-(2-Tetrahydrofuryl)-5-fluorouracil KDMF to evaluate the safety and efficacy of the drug.

After submitting a 1-(2-Tetrahydrofuryl)-5-fluorouracil 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 1-(2-Tetrahydrofuryl)-5-fluorouracil API can apply through the Korea Drug Master File (KDMF).

click here to find a list of 1-(2-Tetrahydrofuryl)-5-fluorouracil suppliers with KDMF on PharmaCompass.

1-(2-Tetrahydrofuryl)-5-fluorouracil WC

A 1-(2-Tetrahydrofuryl)-5-fluorouracil written confirmation (1-(2-Tetrahydrofuryl)-5-fluorouracil WC) is an official document issued by a regulatory agency to a 1-(2-Tetrahydrofuryl)-5-fluorouracil manufacturer, verifying that the manufacturing facility of a 1-(2-Tetrahydrofuryl)-5-fluorouracil active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 1-(2-Tetrahydrofuryl)-5-fluorouracil APIs or 1-(2-Tetrahydrofuryl)-5-fluorouracil finished pharmaceutical products to another nation, regulatory agencies frequently require a 1-(2-Tetrahydrofuryl)-5-fluorouracil WC (written confirmation) as part of the regulatory process.

click here to find a list of 1-(2-Tetrahydrofuryl)-5-fluorouracil suppliers with Written Confirmation (WC) on PharmaCompass.

1-(2-Tetrahydrofuryl)-5-fluorouracil GMP

1-(2-Tetrahydrofuryl)-5-fluorouracil 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 1-(2-Tetrahydrofuryl)-5-fluorouracil 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 1-(2-Tetrahydrofuryl)-5-fluorouracil GMP manufacturer or 1-(2-Tetrahydrofuryl)-5-fluorouracil GMP API supplier for your needs.

1-(2-Tetrahydrofuryl)-5-fluorouracil CoA

A 1-(2-Tetrahydrofuryl)-5-fluorouracil CoA (Certificate of Analysis) is a formal document that attests to 1-(2-Tetrahydrofuryl)-5-fluorouracil's compliance with 1-(2-Tetrahydrofuryl)-5-fluorouracil specifications and serves as a tool for batch-level quality control.

1-(2-Tetrahydrofuryl)-5-fluorouracil CoA mostly includes findings from lab analyses of a specific batch. For each 1-(2-Tetrahydrofuryl)-5-fluorouracil 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.

1-(2-Tetrahydrofuryl)-5-fluorouracil may be tested according to a variety of international standards, such as European Pharmacopoeia (1-(2-Tetrahydrofuryl)-5-fluorouracil EP), 1-(2-Tetrahydrofuryl)-5-fluorouracil JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1-(2-Tetrahydrofuryl)-5-fluorouracil 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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