API Suppliers
US DMFs Filed
CEP/COS Certifications
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JDMFs Filed
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Other Certificates
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Other Suppliers
USA (Orange Book)
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Europe
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Canada
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Australia
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South Africa
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Uploaded Dossiers
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U.S. Medicaid
Annual Reports
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PharmaCompass offers a list of Vilazodone 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 Vilazodone manufacturer or Vilazodone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vilazodone manufacturer or Vilazodone supplier.
PharmaCompass also assists you with knowing the Vilazodone API Price utilized in the formulation of products. Vilazodone API Price is not always fixed or binding as the Vilazodone Price is obtained through a variety of data sources. The Vilazodone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vilazodone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vilazodone, including repackagers and relabelers. The FDA regulates Vilazodone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vilazodone 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 Vilazodone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vilazodone supplier is an individual or a company that provides Vilazodone active pharmaceutical ingredient (API) or Vilazodone finished formulations upon request. The Vilazodone suppliers may include Vilazodone API manufacturers, exporters, distributors and traders.
click here to find a list of Vilazodone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vilazodone DMF (Drug Master File) is a document detailing the whole manufacturing process of Vilazodone active pharmaceutical ingredient (API) in detail. Different forms of Vilazodone DMFs exist exist since differing nations have different regulations, such as Vilazodone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vilazodone DMF submitted to regulatory agencies in the US is known as a USDMF. Vilazodone USDMF includes data on Vilazodone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vilazodone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vilazodone suppliers with USDMF on PharmaCompass.
Vilazodone 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 Vilazodone 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 Vilazodone GMP manufacturer or Vilazodone GMP API supplier for your needs.
A Vilazodone CoA (Certificate of Analysis) is a formal document that attests to Vilazodone's compliance with Vilazodone specifications and serves as a tool for batch-level quality control.
Vilazodone CoA mostly includes findings from lab analyses of a specific batch. For each Vilazodone 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.
Vilazodone may be tested according to a variety of international standards, such as European Pharmacopoeia (Vilazodone EP), Vilazodone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vilazodone USP).