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1. Lp-284
2. Schembl23592489
3. Hy-139453a
4. Cs-0615175
| Molecular Weight | 304.34 g/mol |
|---|---|
| Molecular Formula | C16H20N2O4 |
| XLogP3 | -1.1 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 104 |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 697 |
| 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
A LP-284 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LP-284, including repackagers and relabelers. The FDA regulates LP-284 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LP-284 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 LP-284 supplier is an individual or a company that provides LP-284 active pharmaceutical ingredient (API) or LP-284 finished formulations upon request. The LP-284 suppliers may include LP-284 API manufacturers, exporters, distributors and traders.
LP-284 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 LP-284 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 LP-284 GMP manufacturer or LP-284 GMP API supplier for your needs.
A LP-284 CoA (Certificate of Analysis) is a formal document that attests to LP-284's compliance with LP-284 specifications and serves as a tool for batch-level quality control.
LP-284 CoA mostly includes findings from lab analyses of a specific batch. For each LP-284 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.
LP-284 may be tested according to a variety of international standards, such as European Pharmacopoeia (LP-284 EP), LP-284 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (LP-284 USP).
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