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