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1. 83930-13-6
2. Somatorelin [inn]
3. Unii-4ur7n9z9mm
4. 4ur7n9z9mm
5. Grf (1-44), Human
6. Dtxsid40232828
7. Growth Hormone-releasing Factor (human)
| Molecular Weight | 5040 g/mol |
|---|---|
| Molecular Formula | C215H358N72O66S |
| XLogP3 | -27.2 |
| Hydrogen Bond Donor Count | 83 |
| Hydrogen Bond Acceptor Count | 76 |
| Rotatable Bond Count | 183 |
| Exact Mass | 5038.6658354 g/mol |
| Monoisotopic Mass | 5036.6591258 g/mol |
| Topological Polar Surface Area | 2360 Ų |
| Heavy Atom Count | 354 |
| Formal Charge | 0 |
| Complexity | 12500 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 44 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
V04CD05
S76 | LUXPHARMA | Pharmaceuticals Marketed in Luxembourg | Pharmaceuticals marketed in Luxembourg, as published by d'Gesondheetskeess (CNS, la caisse nationale de sante, www.cns.lu), mapped by name to structures using CompTox by R. Singh et al. (in prep.). List downloaded from https://cns.public.lu/en/legislations/textes-coordonnes/liste-med-comm.html. Dataset DOI:10.5281/zenodo.4587355
V - Various
V04 - Diagnostic agents
V04C - Other diagnostic agents
V04CD - Tests for pituitary function
V04CD05 - Somatorelin
Global Sales Information
ABOUT THIS PAGE
A Somatorelin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Somatorelin, including repackagers and relabelers. The FDA regulates Somatorelin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Somatorelin 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 Somatorelin supplier is an individual or a company that provides Somatorelin active pharmaceutical ingredient (API) or Somatorelin finished formulations upon request. The Somatorelin suppliers may include Somatorelin API manufacturers, exporters, distributors and traders.
Somatorelin 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 Somatorelin 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 Somatorelin GMP manufacturer or Somatorelin GMP API supplier for your needs.
A Somatorelin CoA (Certificate of Analysis) is a formal document that attests to Somatorelin's compliance with Somatorelin specifications and serves as a tool for batch-level quality control.
Somatorelin CoA mostly includes findings from lab analyses of a specific batch. For each Somatorelin 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.
Somatorelin may be tested according to a variety of international standards, such as European Pharmacopoeia (Somatorelin EP), Somatorelin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Somatorelin USP).
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