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1. Npx800
2. 1693734-80-3
3. Npx809
4. Nxp800
5. Schembl16621389
6. Nxp-800
7. Ex-a6036
8. Cct361814
9. Nsc840362
10. Nsc-840362
11. Hy-145927
12. Cs-0435291
| Molecular Weight | 569.6 g/mol |
|---|---|
| Molecular Formula | C32H32FN5O4 |
| XLogP3 | 3.7 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 7 |
| Exact Mass | 569.24383268 g/mol |
| Monoisotopic Mass | 569.24383268 g/mol |
| Topological Polar Surface Area | 96 Ų |
| Heavy Atom Count | 42 |
| Formal Charge | 0 |
| Complexity | 919 |
| 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
A NXP800 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NXP800, including repackagers and relabelers. The FDA regulates NXP800 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NXP800 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 NXP800 supplier is an individual or a company that provides NXP800 active pharmaceutical ingredient (API) or NXP800 finished formulations upon request. The NXP800 suppliers may include NXP800 API manufacturers, exporters, distributors and traders.
NXP800 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 NXP800 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 NXP800 GMP manufacturer or NXP800 GMP API supplier for your needs.
A NXP800 CoA (Certificate of Analysis) is a formal document that attests to NXP800's compliance with NXP800 specifications and serves as a tool for batch-level quality control.
NXP800 CoA mostly includes findings from lab analyses of a specific batch. For each NXP800 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.
NXP800 may be tested according to a variety of international standards, such as European Pharmacopoeia (NXP800 EP), NXP800 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (NXP800 USP).
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