Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
API
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. Pyrilutamide
2. Schembl1444126
3. Ex-a5504
4. Hy-145451
5. Cs-0374724
6. 1272719-00-2
7. 4-[3-[4-cyano-2-fluoro-3-(trifluoromethyl)phenyl]-5,5-dimethyl-4-oxo-2-sulfanylideneimidazolidin-1-yl]-2-fluoro-n-methylbenzamide
| Molecular Weight | 482.4 g/mol |
|---|---|
| Molecular Formula | C21H15F5N4O2S |
| XLogP3 | 3.7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 3 |
| Exact Mass | 482.08358772 g/mol |
| Monoisotopic Mass | 482.08358772 g/mol |
| Topological Polar Surface Area | 109 Ų |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 873 |
| 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 |
ABOUT THIS PAGE
12
PharmaCompass offers a list of Pyrilutamide 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 Pyrilutamide manufacturer or Pyrilutamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pyrilutamide manufacturer or Pyrilutamide supplier.
PharmaCompass also assists you with knowing the Pyrilutamide API Price utilized in the formulation of products. Pyrilutamide API Price is not always fixed or binding as the Pyrilutamide Price is obtained through a variety of data sources. The Pyrilutamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pyrilutamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pyrilutamide, including repackagers and relabelers. The FDA regulates Pyrilutamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pyrilutamide 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 Pyrilutamide supplier is an individual or a company that provides Pyrilutamide active pharmaceutical ingredient (API) or Pyrilutamide finished formulations upon request. The Pyrilutamide suppliers may include Pyrilutamide API manufacturers, exporters, distributors and traders.
Pyrilutamide 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 Pyrilutamide 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 Pyrilutamide GMP manufacturer or Pyrilutamide GMP API supplier for your needs.
A Pyrilutamide CoA (Certificate of Analysis) is a formal document that attests to Pyrilutamide's compliance with Pyrilutamide specifications and serves as a tool for batch-level quality control.
Pyrilutamide CoA mostly includes findings from lab analyses of a specific batch. For each Pyrilutamide 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.
Pyrilutamide may be tested according to a variety of international standards, such as European Pharmacopoeia (Pyrilutamide EP), Pyrilutamide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pyrilutamide USP).
