API Suppliers
US DMFs Filed
CEP/COS Certifications
JDMFs Filed
Other Certificates
Other Suppliers
USA (Orange Book)
Europe
Canada
Australia
South Africa
Uploaded Dossiers
U.S. Medicaid
Annual Reports
18
PharmaCompass offers a list of Entacapone 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 Entacapone manufacturer or Entacapone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Entacapone manufacturer or Entacapone supplier.
PharmaCompass also assists you with knowing the Entacapone API Price utilized in the formulation of products. Entacapone API Price is not always fixed or binding as the Entacapone Price is obtained through a variety of data sources. The Entacapone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Entacapone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Entacapone, including repackagers and relabelers. The FDA regulates Entacapone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Entacapone 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 Entacapone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Entacapone supplier is an individual or a company that provides Entacapone active pharmaceutical ingredient (API) or Entacapone finished formulations upon request. The Entacapone suppliers may include Entacapone API manufacturers, exporters, distributors and traders.
click here to find a list of Entacapone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Entacapone DMF (Drug Master File) is a document detailing the whole manufacturing process of Entacapone active pharmaceutical ingredient (API) in detail. Different forms of Entacapone DMFs exist exist since differing nations have different regulations, such as Entacapone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Entacapone DMF submitted to regulatory agencies in the US is known as a USDMF. Entacapone USDMF includes data on Entacapone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Entacapone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Entacapone suppliers with USDMF on PharmaCompass.
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 Entacapone Drug Master File in Japan (Entacapone JDMF) empowers Entacapone 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 Entacapone JDMF during the approval evaluation for pharmaceutical products. At the time of Entacapone 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 Entacapone suppliers with JDMF 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 Entacapone Drug Master File in Korea (Entacapone KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Entacapone. The MFDS reviews the Entacapone KDMF as part of the drug registration process and uses the information provided in the Entacapone KDMF to evaluate the safety and efficacy of the drug.
After submitting a Entacapone 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 Entacapone API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Entacapone suppliers with KDMF on PharmaCompass.
A Entacapone CEP of the European Pharmacopoeia monograph is often referred to as a Entacapone Certificate of Suitability (COS). The purpose of a Entacapone CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Entacapone EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Entacapone to their clients by showing that a Entacapone CEP has been issued for it. The manufacturer submits a Entacapone CEP (COS) as part of the market authorization procedure, and it takes on the role of a Entacapone CEP holder for the record. Additionally, the data presented in the Entacapone CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Entacapone DMF.
A Entacapone CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Entacapone 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 Entacapone suppliers with CEP (COS) on PharmaCompass.
A Entacapone written confirmation (Entacapone WC) is an official document issued by a regulatory agency to a Entacapone manufacturer, verifying that the manufacturing facility of a Entacapone active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Entacapone APIs or Entacapone finished pharmaceutical products to another nation, regulatory agencies frequently require a Entacapone WC (written confirmation) as part of the regulatory process.
click here to find a list of Entacapone 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 Entacapone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Entacapone 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 Entacapone 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 Entacapone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Entacapone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Entacapone suppliers with NDC on PharmaCompass.
Entacapone 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 Entacapone 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 Entacapone GMP manufacturer or Entacapone GMP API supplier for your needs.
A Entacapone CoA (Certificate of Analysis) is a formal document that attests to Entacapone's compliance with Entacapone specifications and serves as a tool for batch-level quality control.
Entacapone CoA mostly includes findings from lab analyses of a specific batch. For each Entacapone 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.
Entacapone may be tested according to a variety of international standards, such as European Pharmacopoeia (Entacapone EP), Entacapone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Entacapone USP).