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1. Endrysone
2. 35100-44-8
3. Endrysone [usan]
4. Endrisone [inn]
5. 1qz096eief
6. (6s,8s,9s,10r,11s,13s,14s,17s)-17-acetyl-11-hydroxy-6,10,13-trimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
7. Endrisona
8. Endrisonum
9. Endrisona [spanish]
10. Endrisonum [inn-latin]
11. Endrisona [inn-spanish]
12. Unii-1qz096eief
13. Aldrisone
14. Einecs 252-362-6
15. Endrysone (usan/inn)
16. Endrisone [mart.]
17. Schembl43713
18. Chembl2104631
19. 11beta-hydroxy-6alpha-methylpregna-1,4-diene-3,20-dione
20. Dtxsid401043364
21. Zinc4213110
22. Pregna-1,4-diene-3,20-dione, 11-hydroxy-6-methyl-, (6.alpha.,11.beta.)-
23. D03995
24. Q27252771
25. 11.beta.-hydroxy-6.alpha.-methylpregna-1,4-diene-3,20-dione
26. Pregna-1,4-diene-3,20-dione, 11-hydroxy-6-methyl-, (6alpha,11beta)-
| Molecular Weight | 342.5 g/mol |
|---|---|
| Molecular Formula | C22H30O3 |
| XLogP3 | 2.9 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 1 |
| Exact Mass | 342.21949481 g/mol |
| Monoisotopic Mass | 342.21949481 g/mol |
| Topological Polar Surface Area | 54.4 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 689 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 8 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A Endrysone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Endrysone, including repackagers and relabelers. The FDA regulates Endrysone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Endrysone 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 Endrysone supplier is an individual or a company that provides Endrysone active pharmaceutical ingredient (API) or Endrysone finished formulations upon request. The Endrysone suppliers may include Endrysone API manufacturers, exporters, distributors and traders.
click here to find a list of Endrysone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Endrysone DMF (Drug Master File) is a document detailing the whole manufacturing process of Endrysone active pharmaceutical ingredient (API) in detail. Different forms of Endrysone DMFs exist exist since differing nations have different regulations, such as Endrysone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Endrysone DMF submitted to regulatory agencies in the US is known as a USDMF. Endrysone USDMF includes data on Endrysone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Endrysone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Endrysone suppliers with USDMF on PharmaCompass.
Endrysone 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 Endrysone 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 Endrysone GMP manufacturer or Endrysone GMP API supplier for your needs.
A Endrysone CoA (Certificate of Analysis) is a formal document that attests to Endrysone's compliance with Endrysone specifications and serves as a tool for batch-level quality control.
Endrysone CoA mostly includes findings from lab analyses of a specific batch. For each Endrysone 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.
Endrysone may be tested according to a variety of international standards, such as European Pharmacopoeia (Endrysone EP), Endrysone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Endrysone USP).
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