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1. Prax-562
2. 2392951-29-8
3. 3-[ethoxy(difluoro)methyl]-6-[5-fluoro-6-(2,2,2-trifluoroethoxy)pyridin-3-yl]-[1,2,4]triazolo[4,3-a]pyrazine
4. Relutrigine [inn]
5. Aw5c5xhm4w
6. Prax562
7. Chembl5314479
8. Schembl23132181
9. Gtpl12643
10. Bfxbsymvtnefrf-uhfffaoysa-n
11. Glxc-27908
12. Ex-a7203
13. Da-77040
14. Hy-148792
15. Cs-0641132
16. 1,2,4-triazolo(4,3-a)pyrazine, 3-(ethoxydifluoromethyl)-6-(5-fluoro-6-(2,2,2-trifluoroethoxy)-3-pyridinyl)-
17. 3-(ethoxydifluoromethyl)-6-[5-fluoro-6-(2,2,2-trifluoroethoxy)pyridin-3- Yl][1,2,4]triazolo[4,3-a]pyrazine
| Molecular Weight | 407.27 g/mol |
|---|---|
| Molecular Formula | C15H11F6N5O2 |
| XLogP3 | 3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 6 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 74.4 |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 528 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Relutrigine 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 Relutrigine manufacturer or Relutrigine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Relutrigine manufacturer or Relutrigine supplier.
PharmaCompass also assists you with knowing the Relutrigine API Price utilized in the formulation of products. Relutrigine API Price is not always fixed or binding as the Relutrigine Price is obtained through a variety of data sources. The Relutrigine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Relutrigine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Relutrigine, including repackagers and relabelers. The FDA regulates Relutrigine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Relutrigine 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 Relutrigine supplier is an individual or a company that provides Relutrigine active pharmaceutical ingredient (API) or Relutrigine finished formulations upon request. The Relutrigine suppliers may include Relutrigine API manufacturers, exporters, distributors and traders.
Relutrigine 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 Relutrigine 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 Relutrigine GMP manufacturer or Relutrigine GMP API supplier for your needs.
A Relutrigine CoA (Certificate of Analysis) is a formal document that attests to Relutrigine's compliance with Relutrigine specifications and serves as a tool for batch-level quality control.
Relutrigine CoA mostly includes findings from lab analyses of a specific batch. For each Relutrigine 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.
Relutrigine may be tested according to a variety of international standards, such as European Pharmacopoeia (Relutrigine EP), Relutrigine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Relutrigine USP).
