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