Synopsis
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| Molecular Weight | 283.24 g/mol |
|---|---|
| Molecular Formula | C10H13N5O5 |
| XLogP3 | -2.7 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 2 |
| Exact Mass | 283.09166853 g/mol |
| Monoisotopic Mass | 283.09166853 g/mol |
| Topological Polar Surface Area | 155 A^2 |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 446 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
API SUPPLIERS
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USDMF
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ABOUT THIS PAGE
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PharmaCompass offers a list of Guanosine 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 Guanosine manufacturer or Guanosine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Guanosine manufacturer or Guanosine supplier.
PharmaCompass also assists you with knowing the Guanosine API Price utilized in the formulation of products. Guanosine API Price is not always fixed or binding as the Guanosine Price is obtained through a variety of data sources. The Guanosine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Guanosine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Guanosine, including repackagers and relabelers. The FDA regulates Guanosine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Guanosine 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 Guanosine supplier is an individual or a company that provides Guanosine active pharmaceutical ingredient (API) or Guanosine finished formulations upon request. The Guanosine suppliers may include Guanosine API manufacturers, exporters, distributors and traders.
click here to find a list of Guanosine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Guanosine DMF (Drug Master File) is a document detailing the whole manufacturing process of Guanosine active pharmaceutical ingredient (API) in detail. Different forms of Guanosine DMFs exist exist since differing nations have different regulations, such as Guanosine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Guanosine DMF submitted to regulatory agencies in the US is known as a USDMF. Guanosine USDMF includes data on Guanosine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Guanosine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Guanosine suppliers with USDMF on PharmaCompass.
Guanosine 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 Guanosine 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 Guanosine GMP manufacturer or Guanosine GMP API supplier for your needs.
A Guanosine CoA (Certificate of Analysis) is a formal document that attests to Guanosine's compliance with Guanosine specifications and serves as a tool for batch-level quality control.
Guanosine CoA mostly includes findings from lab analyses of a specific batch. For each Guanosine 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.
Guanosine may be tested according to a variety of international standards, such as European Pharmacopoeia (Guanosine EP), Guanosine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Guanosine USP).
