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1. Vit-2763
1. Vit-2763
2. 2095668-10-1
3. Vamifeport [inn]
4. Vamifeport [usan]
5. Fuf66ud0kr
6. 2-[2-[2-(1h-benzimidazol-2-yl)ethylamino]ethyl]-n-[(3-fluoropyridin-2-yl)methyl]-1,3-oxazole-4-carboxamide
7. Vit-2763-pm1
8. 2-(2-((2-(1h-benzimidazol-2-yl)ethyl)amino)ethyl)-n-((3-fluoropyridin-2-yl)methyl)-1,3-oxazole-4-carboxamide
9. 4-oxazolecarboxamide, 2-(2-((2-(1h-benzimidazol-2-yl)ethyl)amino)ethyl)-n-((3-fluoro-2-pyridinyl)methyl)-
10. Unii-fuf66ud0kr
11. Chembl4596566
12. Schembl18764615
13. Gtpl11183
14. Vit2763
15. Ex-a4401
16. Vit 2763
17. Who 11410
18. Hy-112220
19. Cs-0044182
| Molecular Weight | 408.4 g/mol |
|---|---|
| Molecular Formula | C21H21FN6O2 |
| XLogP3 | 1.9 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 9 |
| Exact Mass | 408.17100210 g/mol |
| Monoisotopic Mass | 408.17100210 g/mol |
| Topological Polar Surface Area | 109 Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 556 |
| 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
80
PharmaCompass offers a list of Vamifeport 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 Vamifeport manufacturer or Vamifeport supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vamifeport manufacturer or Vamifeport supplier.
PharmaCompass also assists you with knowing the Vamifeport API Price utilized in the formulation of products. Vamifeport API Price is not always fixed or binding as the Vamifeport Price is obtained through a variety of data sources. The Vamifeport Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vamifeport manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vamifeport, including repackagers and relabelers. The FDA regulates Vamifeport manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vamifeport 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 Vamifeport supplier is an individual or a company that provides Vamifeport active pharmaceutical ingredient (API) or Vamifeport finished formulations upon request. The Vamifeport suppliers may include Vamifeport API manufacturers, exporters, distributors and traders.
Vamifeport 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 Vamifeport 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 Vamifeport GMP manufacturer or Vamifeport GMP API supplier for your needs.
A Vamifeport CoA (Certificate of Analysis) is a formal document that attests to Vamifeport's compliance with Vamifeport specifications and serves as a tool for batch-level quality control.
Vamifeport CoA mostly includes findings from lab analyses of a specific batch. For each Vamifeport 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.
Vamifeport may be tested according to a variety of international standards, such as European Pharmacopoeia (Vamifeport EP), Vamifeport JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vamifeport USP).
