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1. Unii-1pqn78p4s3
2. Opc-167832
3. 1883747-71-4
4. 1pqn78p4s3
5. 5-[[(3r,4r)-1-(4-chloro-2,6-difluorophenyl)-3,4-dihydroxypiperidin-4-yl]methoxy]-8-fluoro-3,4-dihydro-1h-quinolin-2-one
6. Quabodepistat
7. Quabodepistat [inn]
8. Schembl17543112
9. Hy-134940
10. Cs-0167322
11. 2(1h)-quinolinone, 5-(((3r,4r)-1-(4-chloro-2,6-difluorophenyl)-3,4-dihydroxy-4-piperidinyl)methoxy)-8-fluoro-3,4-dihydro-
| Molecular Weight | 456.8 g/mol |
|---|---|
| Molecular Formula | C21H20ClF3N2O4 |
| XLogP3 | 2.5 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 4 |
| Exact Mass | 456.1063693 g/mol |
| Monoisotopic Mass | 456.1063693 g/mol |
| Topological Polar Surface Area | 82 Ų |
| Heavy Atom Count | 31 |
| Formal Charge | 0 |
| Complexity | 652 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A OPC-167832 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of OPC-167832, including repackagers and relabelers. The FDA regulates OPC-167832 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. OPC-167832 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 OPC-167832 supplier is an individual or a company that provides OPC-167832 active pharmaceutical ingredient (API) or OPC-167832 finished formulations upon request. The OPC-167832 suppliers may include OPC-167832 API manufacturers, exporters, distributors and traders.
OPC-167832 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 OPC-167832 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 OPC-167832 GMP manufacturer or OPC-167832 GMP API supplier for your needs.
A OPC-167832 CoA (Certificate of Analysis) is a formal document that attests to OPC-167832's compliance with OPC-167832 specifications and serves as a tool for batch-level quality control.
OPC-167832 CoA mostly includes findings from lab analyses of a specific batch. For each OPC-167832 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.
OPC-167832 may be tested according to a variety of international standards, such as European Pharmacopoeia (OPC-167832 EP), OPC-167832 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (OPC-167832 USP).
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