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1. Teslexivir [inn]
2. 1075798-37-6
3. Sz91e95340
4. 4-[2-[2-(4-benzylphenyl)-2-(2-methyl-6-piperidin-1-ylphenyl)hydrazinyl]-2-oxoethyl]-5-bromo-2-methoxybenzoic Acid
5. Benzeneacetic Acid, 2-bromo-4-carboxy-5-methoxy-, 1-(2-(2-methyl-6-(1-piperidinyl)phenyl)-2-(4-(phenylmethyl)phenyl)hydrazide)
6. Schembl15252044
7. Unii-sz91e95340
8. Hy-109045
9. Cs-0031489
| Molecular Weight | 642.6 g/mol |
|---|---|
| Molecular Formula | C35H36BrN3O4 |
| XLogP3 | 8.1 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 10 |
| Exact Mass | 641.18892 g/mol |
| Monoisotopic Mass | 641.18892 g/mol |
| Topological Polar Surface Area | 82.1 Ų |
| Heavy Atom Count | 43 |
| Formal Charge | 0 |
| Complexity | 886 |
| 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 |
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PharmaCompass offers a list of Teslexivir 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 Teslexivir manufacturer or Teslexivir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Teslexivir manufacturer or Teslexivir supplier.
A Teslexivir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Teslexivir, including repackagers and relabelers. The FDA regulates Teslexivir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Teslexivir 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 Teslexivir supplier is an individual or a company that provides Teslexivir active pharmaceutical ingredient (API) or Teslexivir finished formulations upon request. The Teslexivir suppliers may include Teslexivir API manufacturers, exporters, distributors and traders.
Teslexivir 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 Teslexivir GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Teslexivir GMP manufacturer or Teslexivir GMP API supplier for your needs.
A Teslexivir CoA (Certificate of Analysis) is a formal document that attests to Teslexivir's compliance with Teslexivir specifications and serves as a tool for batch-level quality control.
Teslexivir CoA mostly includes findings from lab analyses of a specific batch. For each Teslexivir 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.
Teslexivir may be tested according to a variety of international standards, such as European Pharmacopoeia (Teslexivir EP), Teslexivir JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Teslexivir USP).
