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1. Appertex
2. R 62690
3. R-62690
1. 101831-36-1
2. R-62690
3. R62,690
4. O8w0r05772
5. (2-chloro-4-(4,5-dihydro-3,5-dioxo-as-triazin-2(3h)-yl)phenyl)(p-chlorophenyl)acetonitrile
6. 2-[2-chloro-4-(3,5-dioxo-1,2,4-triazin-2-yl)phenyl]-2-(4-chlorophenyl)acetonitrile
7. Clazurilum
8. Clazurilo
9. 2-(2-chloro-4-(3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3h)-yl)phenyl)-2-(4-chlorophenyl)acetonitrile
10. Clazurilum [latin]
11. Clazurilo [spanish]
12. Clazuril [usan:inn:ban]
13. Unii-o8w0r05772
14. R 62690
15. Clazuril [usan]
16. Clazuril (usan/inn)
17. Clazuril [inn]
18. Clazuril [mi]
19. Clazuril [mart.]
20. (+/-)-clazuril
21. Schembl466311
22. Clazuril For System Suitability
23. Chembl2104190
24. Clazuril, (+/-)-
25. Dtxsid30869364
26. [2-chloro-4-(3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3h)-yl)phenyl](4-chlorophenyl)acetonitrile
27. Hy-101000
28. Cs-0018222
29. D03533
30. Q3680360
31. 2-chloro-alpha-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3h)-yl)benzeneacetonitrile
32. 2-chloro-alpha-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2-(3h)-yl)benzeneacetonitrile
33. Benzeneacetonitrile, 2-chloro-.alpha.-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3h)-yl)-
| Molecular Weight | 373.2 g/mol |
|---|---|
| Molecular Formula | C17H10Cl2N4O2 |
| XLogP3 | 3.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 3 |
| Exact Mass | 372.0180810 g/mol |
| Monoisotopic Mass | 372.0180810 g/mol |
| Topological Polar Surface Area | 85.6 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 609 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
API SUPPLIERS
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USDMF
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| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
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PharmaCompass offers a list of Clazuril 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 Clazuril manufacturer or Clazuril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clazuril manufacturer or Clazuril supplier.
PharmaCompass also assists you with knowing the Clazuril API Price utilized in the formulation of products. Clazuril API Price is not always fixed or binding as the Clazuril Price is obtained through a variety of data sources. The Clazuril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Appertex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Appertex, including repackagers and relabelers. The FDA regulates Appertex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Appertex 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 Appertex supplier is an individual or a company that provides Appertex active pharmaceutical ingredient (API) or Appertex finished formulations upon request. The Appertex suppliers may include Appertex API manufacturers, exporters, distributors and traders.
click here to find a list of Appertex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Appertex DMF (Drug Master File) is a document detailing the whole manufacturing process of Appertex active pharmaceutical ingredient (API) in detail. Different forms of Appertex DMFs exist exist since differing nations have different regulations, such as Appertex USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Appertex DMF submitted to regulatory agencies in the US is known as a USDMF. Appertex USDMF includes data on Appertex's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Appertex USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Appertex suppliers with USDMF on PharmaCompass.
A Appertex CEP of the European Pharmacopoeia monograph is often referred to as a Appertex Certificate of Suitability (COS). The purpose of a Appertex CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Appertex EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Appertex to their clients by showing that a Appertex CEP has been issued for it. The manufacturer submits a Appertex CEP (COS) as part of the market authorization procedure, and it takes on the role of a Appertex CEP holder for the record. Additionally, the data presented in the Appertex CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Appertex DMF.
A Appertex CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Appertex CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Appertex suppliers with CEP (COS) on PharmaCompass.
Appertex 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 Appertex 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 Appertex GMP manufacturer or Appertex GMP API supplier for your needs.
A Appertex CoA (Certificate of Analysis) is a formal document that attests to Appertex's compliance with Appertex specifications and serves as a tool for batch-level quality control.
Appertex CoA mostly includes findings from lab analyses of a specific batch. For each Appertex 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.
Appertex may be tested according to a variety of international standards, such as European Pharmacopoeia (Appertex EP), Appertex JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Appertex USP).
