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