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1. Eosin Yellowish
2. Schembl18834103
3. Eosin Y Solution, 5 Wt. % In H2o
4. Eosin Y Disodium Salt, For Electrophoresis
5. Eosin Y, Saj Special Grade, >=85.0%
6. Eosin Y Disodium Salt, Dye Content >=85 %
7. Eosin Y Disodium Salt, Certified By The Biological Stain Commission
8. Eosin Y Disodium Salt, For Microscopy (fl., Hist.), Adsorption And Fluorescent Indicator
| Molecular Weight | 693.9 g/mol |
|---|---|
| Molecular Formula | C20H8Br4Na2O5 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 2 |
| Exact Mass | 693.68596 g/mol |
| Monoisotopic Mass | 689.69006 g/mol |
| Topological Polar Surface Area | 83.8 Ų |
| Heavy Atom Count | 31 |
| Formal Charge | 0 |
| Complexity | 848 |
| 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 | 3 |
ABOUT THIS PAGE
A Eosin Yellowish manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eosin Yellowish, including repackagers and relabelers. The FDA regulates Eosin Yellowish manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eosin Yellowish 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 Eosin Yellowish manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eosin Yellowish supplier is an individual or a company that provides Eosin Yellowish active pharmaceutical ingredient (API) or Eosin Yellowish finished formulations upon request. The Eosin Yellowish suppliers may include Eosin Yellowish API manufacturers, exporters, distributors and traders.
click here to find a list of Eosin Yellowish suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Eosin Yellowish written confirmation (Eosin Yellowish WC) is an official document issued by a regulatory agency to a Eosin Yellowish manufacturer, verifying that the manufacturing facility of a Eosin Yellowish active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Eosin Yellowish APIs or Eosin Yellowish finished pharmaceutical products to another nation, regulatory agencies frequently require a Eosin Yellowish WC (written confirmation) as part of the regulatory process.
click here to find a list of Eosin Yellowish suppliers with Written Confirmation (WC) on PharmaCompass.
Eosin Yellowish 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 Eosin Yellowish 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 Eosin Yellowish GMP manufacturer or Eosin Yellowish GMP API supplier for your needs.
A Eosin Yellowish CoA (Certificate of Analysis) is a formal document that attests to Eosin Yellowish's compliance with Eosin Yellowish specifications and serves as a tool for batch-level quality control.
Eosin Yellowish CoA mostly includes findings from lab analyses of a specific batch. For each Eosin Yellowish 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.
Eosin Yellowish may be tested according to a variety of international standards, such as European Pharmacopoeia (Eosin Yellowish EP), Eosin Yellowish JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Eosin Yellowish USP).
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