US DMFs Filed
USA (Orange Book)
PharmaCompass offers a list of Capecitabine 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 Capecitabine manufacturer or Capecitabine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Capecitabine manufacturer or Capecitabine supplier.
PharmaCompass also assists you with knowing the Capecitabine API Price utilized in the formulation of products. Capecitabine API Price is not always fixed or binding as the Capecitabine Price is obtained through a variety of data sources. The Capecitabine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Capecitabine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Capecitabine, including repackagers and relabelers. The FDA regulates Capecitabine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Capecitabine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Capecitabine supplier is an individual or a company that provides Capecitabine active pharmaceutical ingredient (API) or Capecitabine finished formulations upon request. The Capecitabine suppliers may include Capecitabine API manufacturers, exporters, distributors and traders.
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A Capecitabine DMF (Drug Master File) is a document detailing the whole manufacturing process of Capecitabine active pharmaceutical ingredient (API) in detail. Different forms of Capecitabine DMFs exist exist since differing nations have different regulations, such as Capecitabine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Capecitabine DMF submitted to regulatory agencies in the US is known as a USDMF. Capecitabine USDMF includes data on Capecitabine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Capecitabine USDMF is kept confidential to protect the manufacturer’s intellectual property.
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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 Capecitabine Drug Master File in Japan (Capecitabine JDMF) empowers Capecitabine 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 Capecitabine JDMF during the approval evaluation for pharmaceutical products. At the time of Capecitabine JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Capecitabine Drug Master File in Korea (Capecitabine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Capecitabine. The MFDS reviews the Capecitabine KDMF as part of the drug registration process and uses the information provided in the Capecitabine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Capecitabine 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 Capecitabine API can apply through the Korea Drug Master File (KDMF).
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A Capecitabine CEP of the European Pharmacopoeia monograph is often referred to as a Capecitabine Certificate of Suitability (COS). The purpose of a Capecitabine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Capecitabine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Capecitabine to their clients by showing that a Capecitabine CEP has been issued for it. The manufacturer submits a Capecitabine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Capecitabine CEP holder for the record. Additionally, the data presented in the Capecitabine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Capecitabine DMF.
A Capecitabine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Capecitabine CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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A Capecitabine written confirmation (Capecitabine WC) is an official document issued by a regulatory agency to a Capecitabine manufacturer, verifying that the manufacturing facility of a Capecitabine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Capecitabine APIs or Capecitabine finished pharmaceutical products to another nation, regulatory agencies frequently require a Capecitabine WC (written confirmation) as part of the regulatory process.
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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 Capecitabine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Capecitabine 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 Capecitabine 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 Capecitabine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Capecitabine NDC to their finished compounded human drug products, they may choose to do so.
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Capecitabine 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 Capecitabine 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 Capecitabine GMP manufacturer or Capecitabine GMP API supplier for your needs.
A Capecitabine CoA (Certificate of Analysis) is a formal document that attests to Capecitabine's compliance with Capecitabine specifications and serves as a tool for batch-level quality control.
Capecitabine CoA mostly includes findings from lab analyses of a specific batch. For each Capecitabine 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.
Capecitabine may be tested according to a variety of international standards, such as European Pharmacopoeia (Capecitabine EP), Capecitabine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Capecitabine USP).