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1. Unii-x6466m4lvp
2. 2055496-11-0
3. Cedirogant [inn]
4. Cedirogant [usan]
5. Abbv-157
6. X6466m4lvp
7. (1-(2,4-dichloro-3-((7-chloro-5-(trifluoromethyl)-1hindol-1-yl)methyl)benzoyl)piperidin-4-yl)acetic Acid
8. 2-[1-[2,4-dichloro-3-[[7-chloro-5-(trifluoromethyl)indol-1-yl]methyl]benzoyl]piperidin-4-yl]acetic Acid
9. 4-piperidineacetic Acid, 1-(2,4-dichloro-3-((7-chloro-5-(trifluoromethyl)-1h-indol-1-yl)methyl)benzoyl)-
10. Schembl18299842
11. Abv-157
12. Bdbm292795
13. Ex-a5810
14. Us10106501, Example Ei-5
15. Us10106501, Example Ei-6
16. Who 11460
17. Hy-137434
18. Cs-0138634
19. F77949
20. 2-(1-(2,4-dichloro-3-((7-chloro-5-(trifluoromethyl)-1h-indol-1-yl)methyl)benzoyl)piperidin-4-yl)acetic Acid
| Molecular Weight | 547.8 g/mol |
|---|---|
| Molecular Formula | C24H20Cl3F3N2O3 |
| XLogP3 | 6.1 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 5 |
| Exact Mass | 546.049160 g/mol |
| Monoisotopic Mass | 546.049160 g/mol |
| Topological Polar Surface Area | 62.5 Ų |
| Heavy Atom Count | 35 |
| Formal Charge | 0 |
| Complexity | 781 |
| 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 |
Drugs in Development
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PharmaCompass offers a list of Cedirogant API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Cedirogant manufacturer or Cedirogant supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cedirogant manufacturer or Cedirogant supplier.
PharmaCompass also assists you with knowing the Cedirogant API Price utilized in the formulation of products. Cedirogant API Price is not always fixed or binding as the Cedirogant Price is obtained through a variety of data sources. The Cedirogant Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cedirogant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cedirogant, including repackagers and relabelers. The FDA regulates Cedirogant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cedirogant 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 Cedirogant supplier is an individual or a company that provides Cedirogant active pharmaceutical ingredient (API) or Cedirogant finished formulations upon request. The Cedirogant suppliers may include Cedirogant API manufacturers, exporters, distributors and traders.
Cedirogant 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 Cedirogant 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 Cedirogant GMP manufacturer or Cedirogant GMP API supplier for your needs.
A Cedirogant CoA (Certificate of Analysis) is a formal document that attests to Cedirogant's compliance with Cedirogant specifications and serves as a tool for batch-level quality control.
Cedirogant CoA mostly includes findings from lab analyses of a specific batch. For each Cedirogant 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.
Cedirogant may be tested according to a variety of international standards, such as European Pharmacopoeia (Cedirogant EP), Cedirogant JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cedirogant USP).
