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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EDQM
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USP
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JP
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Others
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Medicaid
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1. Oxidase, Urate
2. Urate Oxidase
3. Uricase
1. 9002-12-4
2. Azane;[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl [5-(2,4-dioxopyrimidin-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] Hydrogen Phosphate
3. Oxidase, Urate
4. Uricase, Candida Utilis
5. Mfcd00082126
6. Ft-0686693
7. Ft-0772402
8. Uricase From Bacillus Fastidiosus, Lyophilized, ~9 U/mg
9. Uricase From Arthrobacter Globiformis, Lyophilized Powder, 15-30 Units/mg Protein (biuret)
10. Uricase From Candida Sp., Recombinant, Expressed In E. Coli, Lyophilized Powder, >=2 Units/mg Solid
Molecular Weight | 567.4 g/mol |
---|---|
Molecular Formula | C18H26N5O14P |
Hydrogen Bond Donor Count | 8 |
Hydrogen Bond Acceptor Count | 15 |
Rotatable Bond Count | 8 |
Exact Mass | 567.12138752 g/mol |
Monoisotopic Mass | 567.12138752 g/mol |
Topological Polar Surface Area | 255 Ų |
Heavy Atom Count | 38 |
Formal Charge | 0 |
Complexity | 1070 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 8 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
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PharmaCompass offers a list of Urate Oxidase 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 Urate Oxidase manufacturer or Urate Oxidase supplier for your needs.
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A Uricase from Arthrobacter globiformis manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uricase from Arthrobacter globiformis, including repackagers and relabelers. The FDA regulates Uricase from Arthrobacter globiformis manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uricase from Arthrobacter globiformis 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 Uricase from Arthrobacter globiformis manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Uricase from Arthrobacter globiformis supplier is an individual or a company that provides Uricase from Arthrobacter globiformis active pharmaceutical ingredient (API) or Uricase from Arthrobacter globiformis finished formulations upon request. The Uricase from Arthrobacter globiformis suppliers may include Uricase from Arthrobacter globiformis API manufacturers, exporters, distributors and traders.
click here to find a list of Uricase from Arthrobacter globiformis suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Uricase from Arthrobacter globiformis DMF (Drug Master File) is a document detailing the whole manufacturing process of Uricase from Arthrobacter globiformis active pharmaceutical ingredient (API) in detail. Different forms of Uricase from Arthrobacter globiformis DMFs exist exist since differing nations have different regulations, such as Uricase from Arthrobacter globiformis USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Uricase from Arthrobacter globiformis DMF submitted to regulatory agencies in the US is known as a USDMF. Uricase from Arthrobacter globiformis USDMF includes data on Uricase from Arthrobacter globiformis's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Uricase from Arthrobacter globiformis USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Uricase from Arthrobacter globiformis suppliers with USDMF on PharmaCompass.
Uricase from Arthrobacter globiformis 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 Uricase from Arthrobacter globiformis 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 Uricase from Arthrobacter globiformis GMP manufacturer or Uricase from Arthrobacter globiformis GMP API supplier for your needs.
A Uricase from Arthrobacter globiformis CoA (Certificate of Analysis) is a formal document that attests to Uricase from Arthrobacter globiformis's compliance with Uricase from Arthrobacter globiformis specifications and serves as a tool for batch-level quality control.
Uricase from Arthrobacter globiformis CoA mostly includes findings from lab analyses of a specific batch. For each Uricase from Arthrobacter globiformis 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.
Uricase from Arthrobacter globiformis may be tested according to a variety of international standards, such as European Pharmacopoeia (Uricase from Arthrobacter globiformis EP), Uricase from Arthrobacter globiformis JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Uricase from Arthrobacter globiformis USP).