Synopsis
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1. Ip2015
2. Ip2015 Free Base
3. 1320346-14-2
4. Ns18313
5. Ns-18313
6. Pudafensina
7. Pudafensine [inn]
8. Ip-2015
9. L9ng7us8ge
10. Orb2564633
11. Chembl6068030
12. Schembl26989874
13. Hy-162511
14. Cs-1054102
15. 2h-1-benzopyran-2-one, 7-[(3-exo)-8-azabicyclo[3.2.1]oct-3-yloxy]-3-methoxy-
16. 7-[(3-exo)-8-azabicyclo[3.2.1]oct-3-yloxy]-3-methoxy-2h-1-benzopyran-2-one
| Molecular Weight | 301.34 g/mol |
|---|---|
| Molecular Formula | C17H19NO4 |
| XLogP3 | 2.8 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 3 |
| Exact Mass | Da |
| Monoisotopic Mass | Da |
| Topological Polar Surface Area | 56.8 |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 465 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| 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 Pudafensine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Pudafensine manufacturer or Pudafensine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pudafensine manufacturer or Pudafensine supplier.
A Pudafensine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pudafensine, including repackagers and relabelers. The FDA regulates Pudafensine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pudafensine 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 Pudafensine supplier is an individual or a company that provides Pudafensine active pharmaceutical ingredient (API) or Pudafensine finished formulations upon request. The Pudafensine suppliers may include Pudafensine API manufacturers, exporters, distributors and traders.
Pudafensine 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 Pudafensine GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Pudafensine GMP manufacturer or Pudafensine GMP API supplier for your needs.
A Pudafensine CoA (Certificate of Analysis) is a formal document that attests to Pudafensine's compliance with Pudafensine specifications and serves as a tool for batch-level quality control.
Pudafensine CoA mostly includes findings from lab analyses of a specific batch. For each Pudafensine 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.
Pudafensine may be tested according to a variety of international standards, such as European Pharmacopoeia (Pudafensine EP), Pudafensine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pudafensine USP).
