Synopsis
Synopsis
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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Listed Suppliers
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EDQM
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USP
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JP
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FDF Dossiers
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FDA Orange Book
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Europe
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US Medicaid
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Data Compilation #PharmaFlow
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News #PharmaBuzz
| Molecular Weight | 220.18 g/mol |
|---|---|
| Molecular Formula | C10H8N2O4 |
| XLogP3 | 1.4 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 3 |
| Exact Mass | 220.04840674 g/mol |
| Monoisotopic Mass | 220.04840674 g/mol |
| Topological Polar Surface Area | 88 A^2 |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 293 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Furildioxime 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 Furildioxime manufacturer or Furildioxime supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Furildioxime manufacturer or Furildioxime supplier.
PharmaCompass also assists you with knowing the Furildioxime API Price utilized in the formulation of products. Furildioxime API Price is not always fixed or binding as the Furildioxime Price is obtained through a variety of data sources. The Furildioxime Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A FURIL DIOXIME manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FURIL DIOXIME, including repackagers and relabelers. The FDA regulates FURIL DIOXIME manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FURIL DIOXIME 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 FURIL DIOXIME supplier is an individual or a company that provides FURIL DIOXIME active pharmaceutical ingredient (API) or FURIL DIOXIME finished formulations upon request. The FURIL DIOXIME suppliers may include FURIL DIOXIME API manufacturers, exporters, distributors and traders.
click here to find a list of FURIL DIOXIME suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A FURIL DIOXIME DMF (Drug Master File) is a document detailing the whole manufacturing process of FURIL DIOXIME active pharmaceutical ingredient (API) in detail. Different forms of FURIL DIOXIME DMFs exist exist since differing nations have different regulations, such as FURIL DIOXIME USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A FURIL DIOXIME DMF submitted to regulatory agencies in the US is known as a USDMF. FURIL DIOXIME USDMF includes data on FURIL DIOXIME's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The FURIL DIOXIME USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of FURIL DIOXIME suppliers with USDMF on PharmaCompass.
FURIL DIOXIME 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 FURIL DIOXIME 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 FURIL DIOXIME GMP manufacturer or FURIL DIOXIME GMP API supplier for your needs.
A FURIL DIOXIME CoA (Certificate of Analysis) is a formal document that attests to FURIL DIOXIME's compliance with FURIL DIOXIME specifications and serves as a tool for batch-level quality control.
FURIL DIOXIME CoA mostly includes findings from lab analyses of a specific batch. For each FURIL DIOXIME 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.
FURIL DIOXIME may be tested according to a variety of international standards, such as European Pharmacopoeia (FURIL DIOXIME EP), FURIL DIOXIME JP (Japanese Pharmacopeia) and the US Pharmacopoeia (FURIL DIOXIME USP).
