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1. 2019-25-2
2. Orpidan
3. Chlorazanil Hcl
4. Chlorazanil (hydrochloride)
5. Doclizid-t
6. Nsc-60256
7. N-(4-chlorophenyl)-1,3,5-triazine-2,4-diamine Monohydrochloride
8. 9961sl881j
9. 2-n-(4-chlorophenyl)-1,3,5-triazine-2,4-diamine;hydrochloride
10. 2-amino-4-p-chloroanilino-s-triazine Hydrochloride
11. Unii-9961sl881j
12. Einecs 217-962-4
13. Chlorazanil Hydrochlorideide
14. Chembl2104101
15. Schembl22207597
16. Dtxsid00942254
17. S-triazine, 2-amino-4-(p-chloroanilino)-, Monohydrochloride
18. Hy-b1045
19. Nsc60256
20. 1,3,5-triazine-2,4-diamine, N-(4-chlorophenyl)-, Monohydrochloride
21. Nsc 60256
22. Chlorazanil Hydrochloride [mi]
23. Akos024332744
24. Cs-4566
25. Chlorazanil Hydrochloride [mart.]
26. Chlorazanil Hydrochloride [who-dd]
27. Q27272176
28. 1,5-triazine-2,4-diamine, N-(4-chlorophenyl)-, Monohydrochloride
29. N-(4-chloro-phenyl)-[1,3,5]triazine-2,4-diamine Hydrochloride
30. N-(4-chlorophenyl)-6-imino-1,6-dihydro-1,3,5-triazin-2-amine--hydrogen Chloride (1/1)
Molecular Weight | 258.10 g/mol |
---|---|
Molecular Formula | C9H9Cl2N5 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 5 |
Rotatable Bond Count | 2 |
Exact Mass | 257.0235007 g/mol |
Monoisotopic Mass | 257.0235007 g/mol |
Topological Polar Surface Area | 76.7 Ų |
Heavy Atom Count | 16 |
Formal Charge | 0 |
Complexity | 195 |
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 | 2 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Orpidan 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 Orpidan manufacturer or Orpidan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Orpidan manufacturer or Orpidan supplier.
PharmaCompass also assists you with knowing the Orpidan API Price utilized in the formulation of products. Orpidan API Price is not always fixed or binding as the Orpidan Price is obtained through a variety of data sources. The Orpidan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Orpidan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Orpidan, including repackagers and relabelers. The FDA regulates Orpidan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Orpidan 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 Orpidan supplier is an individual or a company that provides Orpidan active pharmaceutical ingredient (API) or Orpidan finished formulations upon request. The Orpidan suppliers may include Orpidan API manufacturers, exporters, distributors and traders.
Orpidan 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 Orpidan 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 Orpidan GMP manufacturer or Orpidan GMP API supplier for your needs.
A Orpidan CoA (Certificate of Analysis) is a formal document that attests to Orpidan's compliance with Orpidan specifications and serves as a tool for batch-level quality control.
Orpidan CoA mostly includes findings from lab analyses of a specific batch. For each Orpidan 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.
Orpidan may be tested according to a variety of international standards, such as European Pharmacopoeia (Orpidan EP), Orpidan JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Orpidan USP).