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1. Dtxsid901336869
2. Refchem:1075133
3. Dtxcid001767164
4. Zalsupindole
5. Aaz-a 154
6. Aaz-a154
7. 2481740-94-5
8. (2r)-1-(5-methoxyindol-1-yl)-n,n-dimethylpropan-2-amine
9. Zalsupindole [inn]
10. Orb2664906
11. Schembl23927895
12. Gtpl13552
13. Glxc-26412
14. Ur7446669r
15. Cs-0646791
16. (alphar)-5-methoxy-n,n,alpha-trimethyl-1h-indole-1-ethanamine
17. 1h-indole-1-ethanamine, 5-methoxy-n,n,alpha-trimethyl-, (alphar)-
| Molecular Weight | 232.32 g/mol |
|---|---|
| Molecular Formula | C14H20N2O |
| XLogP3 | 2.4 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 4 |
| Exact Mass | Da |
| Monoisotopic Mass | Da |
| Topological Polar Surface Area | 17.4 |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 244 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| 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 Zalsupindole 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 Zalsupindole manufacturer or Zalsupindole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zalsupindole manufacturer or Zalsupindole supplier.
A Zalsupindole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zalsupindole, including repackagers and relabelers. The FDA regulates Zalsupindole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zalsupindole 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 Zalsupindole supplier is an individual or a company that provides Zalsupindole active pharmaceutical ingredient (API) or Zalsupindole finished formulations upon request. The Zalsupindole suppliers may include Zalsupindole API manufacturers, exporters, distributors and traders.
Zalsupindole 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 Zalsupindole GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Zalsupindole GMP manufacturer or Zalsupindole GMP API supplier for your needs.
A Zalsupindole CoA (Certificate of Analysis) is a formal document that attests to Zalsupindole's compliance with Zalsupindole specifications and serves as a tool for batch-level quality control.
Zalsupindole CoA mostly includes findings from lab analyses of a specific batch. For each Zalsupindole 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.
Zalsupindole may be tested according to a variety of international standards, such as European Pharmacopoeia (Zalsupindole EP), Zalsupindole JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zalsupindole USP).
