Synopsis
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| Molecular Weight | 960.8 g/mol |
|---|---|
| Molecular Formula | C34H24N6Na4O14S4 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 20 |
| Rotatable Bond Count | 5 |
| Exact Mass | 959.9824113 g/mol |
| Monoisotopic Mass | 959.9824113 g/mol |
| Topological Polar Surface Area | 397 Ų |
| Heavy Atom Count | 62 |
| Formal Charge | 0 |
| Complexity | 2000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 5 |
ABOUT THIS PAGE
A Evans Blue manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Evans Blue, including repackagers and relabelers. The FDA regulates Evans Blue manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Evans Blue API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Evans Blue manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Evans Blue supplier is an individual or a company that provides Evans Blue active pharmaceutical ingredient (API) or Evans Blue finished formulations upon request. The Evans Blue suppliers may include Evans Blue API manufacturers, exporters, distributors and traders.
click here to find a list of Evans Blue suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Evans Blue 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 Evans Blue 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 Evans Blue GMP manufacturer or Evans Blue GMP API supplier for your needs.
A Evans Blue CoA (Certificate of Analysis) is a formal document that attests to Evans Blue's compliance with Evans Blue specifications and serves as a tool for batch-level quality control.
Evans Blue CoA mostly includes findings from lab analyses of a specific batch. For each Evans Blue 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.
Evans Blue may be tested according to a variety of international standards, such as European Pharmacopoeia (Evans Blue EP), Evans Blue JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Evans Blue USP).
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