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1. Chembl4099413
2. Schembl18546463
3. Bdbm454169
4. Ex-a8320
5. Bdbm50246180
6. Us10716791, Code Kp-302
7. 2082765-42-0
| Molecular Weight | 365.4 g/mol |
|---|---|
| Molecular Formula | C20H23N5O2 |
| XLogP3 | 1.2 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 8 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 81 |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 495 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Lucid-21-302 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 Lucid-21-302 manufacturer or Lucid-21-302 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lucid-21-302 manufacturer or Lucid-21-302 supplier.
PharmaCompass also assists you with knowing the Lucid-21-302 API Price utilized in the formulation of products. Lucid-21-302 API Price is not always fixed or binding as the Lucid-21-302 Price is obtained through a variety of data sources. The Lucid-21-302 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lucid-21-302 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lucid-21-302, including repackagers and relabelers. The FDA regulates Lucid-21-302 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lucid-21-302 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 Lucid-21-302 supplier is an individual or a company that provides Lucid-21-302 active pharmaceutical ingredient (API) or Lucid-21-302 finished formulations upon request. The Lucid-21-302 suppliers may include Lucid-21-302 API manufacturers, exporters, distributors and traders.
Lucid-21-302 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 Lucid-21-302 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 Lucid-21-302 GMP manufacturer or Lucid-21-302 GMP API supplier for your needs.
A Lucid-21-302 CoA (Certificate of Analysis) is a formal document that attests to Lucid-21-302's compliance with Lucid-21-302 specifications and serves as a tool for batch-level quality control.
Lucid-21-302 CoA mostly includes findings from lab analyses of a specific batch. For each Lucid-21-302 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.
Lucid-21-302 may be tested according to a variety of international standards, such as European Pharmacopoeia (Lucid-21-302 EP), Lucid-21-302 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lucid-21-302 USP).
