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