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1. 84650-00-0
2. Furan;1-methylpyridin-1-ium-3-carboxylate;pyridine-3-carboxylic Acid;1,3,7-trimethyl-4,5-dihydropurine-2,6-dione
3. Coffee, Coffea Arabica, Ext.
Molecular Weight | 524.5 g/mol |
---|---|
Molecular Formula | C25H28N6O7 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 9 |
Rotatable Bond Count | 1 |
Exact Mass | 524.20194725 g/mol |
Monoisotopic Mass | 524.20194725 g/mol |
Topological Polar Surface Area | 164 Ų |
Heavy Atom Count | 38 |
Formal Charge | 0 |
Complexity | 594 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 2 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 4 |
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Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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ABOUT THIS PAGE
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PharmaCompass offers a list of Coffee extract 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 Coffee extract manufacturer or Coffee extract supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Coffee extract manufacturer or Coffee extract supplier.
PharmaCompass also assists you with knowing the Coffee extract API Price utilized in the formulation of products. Coffee extract API Price is not always fixed or binding as the Coffee extract Price is obtained through a variety of data sources. The Coffee extract Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Coffee, Coffea arabica, ext. manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Coffee, Coffea arabica, ext., including repackagers and relabelers. The FDA regulates Coffee, Coffea arabica, ext. manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Coffee, Coffea arabica, ext. API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Coffee, Coffea arabica, ext. supplier is an individual or a company that provides Coffee, Coffea arabica, ext. active pharmaceutical ingredient (API) or Coffee, Coffea arabica, ext. finished formulations upon request. The Coffee, Coffea arabica, ext. suppliers may include Coffee, Coffea arabica, ext. API manufacturers, exporters, distributors and traders.
click here to find a list of Coffee, Coffea arabica, ext. suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Coffee, Coffea arabica, ext. DMF (Drug Master File) is a document detailing the whole manufacturing process of Coffee, Coffea arabica, ext. active pharmaceutical ingredient (API) in detail. Different forms of Coffee, Coffea arabica, ext. DMFs exist exist since differing nations have different regulations, such as Coffee, Coffea arabica, ext. USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Coffee, Coffea arabica, ext. DMF submitted to regulatory agencies in the US is known as a USDMF. Coffee, Coffea arabica, ext. USDMF includes data on Coffee, Coffea arabica, ext.'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Coffee, Coffea arabica, ext. USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Coffee, Coffea arabica, ext. suppliers with USDMF on PharmaCompass.
Coffee, Coffea arabica, ext. 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 Coffee, Coffea arabica, ext. 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 Coffee, Coffea arabica, ext. GMP manufacturer or Coffee, Coffea arabica, ext. GMP API supplier for your needs.
A Coffee, Coffea arabica, ext. CoA (Certificate of Analysis) is a formal document that attests to Coffee, Coffea arabica, ext.'s compliance with Coffee, Coffea arabica, ext. specifications and serves as a tool for batch-level quality control.
Coffee, Coffea arabica, ext. CoA mostly includes findings from lab analyses of a specific batch. For each Coffee, Coffea arabica, ext. 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.
Coffee, Coffea arabica, ext. may be tested according to a variety of international standards, such as European Pharmacopoeia (Coffee, Coffea arabica, ext. EP), Coffee, Coffea arabica, ext. JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Coffee, Coffea arabica, ext. USP).