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Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
Neuland Laboratories- A dedicated 100% API provider.
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
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NDC API
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Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
About the Company : Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product gro...
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
About the Company : Founded in 1984, DRL is well-known for its generic APIs and its track record in drug product development. It is one of the earliest pharma API manufacturers with a diverse portfoli...
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
About the Company : HRV Global is a leading global manufacturer, seller & exporter of a wide range of APIs, advanced intermediates, pellets, food grade chemicals, food additives & food ingredients. It...
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
About the Company : Mankind Pharma, came into existence in 1986. In 1991, the company was formed into a legal corporation. However, it actively started working as a fully integrated pharmaceutical com...
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ABOUT THIS PAGE
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PharmaCompass offers a list of Xanomeline 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 Xanomeline manufacturer or Xanomeline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Xanomeline manufacturer or Xanomeline supplier.
PharmaCompass also assists you with knowing the Xanomeline API Price utilized in the formulation of products. Xanomeline API Price is not always fixed or binding as the Xanomeline Price is obtained through a variety of data sources. The Xanomeline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Xanomeline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xanomeline, including repackagers and relabelers. The FDA regulates Xanomeline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xanomeline 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 Xanomeline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Xanomeline supplier is an individual or a company that provides Xanomeline active pharmaceutical ingredient (API) or Xanomeline finished formulations upon request. The Xanomeline suppliers may include Xanomeline API manufacturers, exporters, distributors and traders.
click here to find a list of Xanomeline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Xanomeline as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Xanomeline 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 Xanomeline 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 Xanomeline and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Xanomeline NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Xanomeline suppliers with NDC on PharmaCompass.
Xanomeline 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 Xanomeline 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 Xanomeline GMP manufacturer or Xanomeline GMP API supplier for your needs.
A Xanomeline CoA (Certificate of Analysis) is a formal document that attests to Xanomeline's compliance with Xanomeline specifications and serves as a tool for batch-level quality control.
Xanomeline CoA mostly includes findings from lab analyses of a specific batch. For each Xanomeline 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.
Xanomeline may be tested according to a variety of international standards, such as European Pharmacopoeia (Xanomeline EP), Xanomeline JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Xanomeline USP).
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