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1. Daypro Alta
2. 174064-08-5
3. Oxaprozin (potassium)
4. Ml56o2z92i
5. Unii-ml56o2z92i
6. Oxaprozin, Potassium Salt
7. Schembl8190699
8. 2-oxazolepropanoic Acid, 4,5-diphenyl-, Potassium Salt
9. Chembl1200463
10. Hy-b0808a
11. Dtxsid70169754
12. Oxaprozin Potassium [mart.]
13. Oxaprozin Potassium [who-dd]
14. Oxaprozin Potassium [orange Book]
15. Cs-0031253
16. Q27284098
17. Potassium;3-(4,5-diphenyl-1,3-oxazol-2-yl)propanoate
| Molecular Weight | 331.4 g/mol |
|---|---|
| Molecular Formula | C18H14KNO3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Exact Mass | 331.06107479 g/mol |
| Monoisotopic Mass | 331.06107479 g/mol |
| Topological Polar Surface Area | 66.2 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 367 |
| 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 | 2 |
ABOUT THIS PAGE
A Oxaprozin Potassium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxaprozin Potassium, including repackagers and relabelers. The FDA regulates Oxaprozin Potassium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxaprozin Potassium 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 Oxaprozin Potassium supplier is an individual or a company that provides Oxaprozin Potassium active pharmaceutical ingredient (API) or Oxaprozin Potassium finished formulations upon request. The Oxaprozin Potassium suppliers may include Oxaprozin Potassium API manufacturers, exporters, distributors and traders.
Oxaprozin Potassium 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 Oxaprozin Potassium 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 Oxaprozin Potassium GMP manufacturer or Oxaprozin Potassium GMP API supplier for your needs.
A Oxaprozin Potassium CoA (Certificate of Analysis) is a formal document that attests to Oxaprozin Potassium's compliance with Oxaprozin Potassium specifications and serves as a tool for batch-level quality control.
Oxaprozin Potassium CoA mostly includes findings from lab analyses of a specific batch. For each Oxaprozin Potassium 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.
Oxaprozin Potassium may be tested according to a variety of international standards, such as European Pharmacopoeia (Oxaprozin Potassium EP), Oxaprozin Potassium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Oxaprozin Potassium USP).
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