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1. 133xe Radioisotope
2. Xe-133 Radioisotope
3. Xenon-133
1. Xenon-133
2. Xenon Xe 133
3. Xenon (133xe)
4. Xenon, Xe-133
5. 14932-42-4
6. Xenon (133 Xe)
7. Xenon (133xe) Gas
8. Xenon 133
9. X3p9a5hnyf
10. Xenon (133xe) [inn]
11. Xeneisol
12. Xenon Xe 133-v.s.s.
13. Xenonum (133 Xe)
14. Unii-x3p9a5hnyf
15. Xenon Xe 133 [usan]
16. Xenon, Isotope Of Mass 133
17. Mpi Xenon Xe 133 Gas Vials
18. Mpi Xenon Xe 133 Gas Ampule
19. Xe-133
20. Xenon Xe 133 [usan:usp]
21. Xenon ((sup 133)xe) Injection
22. Xenon Radioisotopes
23. Xenonum (133 Xe) [inn-latin]
24. 133xe Radioisotope
25. Xe-133 Radioisotope
26. Xenon,xe-133
27. Xenon (133xe) Injection
28. Xenon Xe 133 (tn)
29. Xenon Xe 133 Gas Vials
30. Xenon ((sup 133)xe)
31. Xenon Xe 133 Gas Ampule
32. Chembl1200685
33. Xenon Xe 133 [mi]
34. Xenon-133 [mart.]
35. Dtxsid70933614
36. Xenon,xe-133 [vandf]
37. 133xe
38. Xenon (133xe) [jan]
39. Xenon Xe 133 (jan/usp/inn)
40. Xenon (133 Xe) [who-dd]
41. Xenon Xe-133 [orange Book]
42. Db09315
43. Xenon Xe 133 [usp Monograph]
44. D06339
45. Q2451397
Molecular Weight | 132.90591 g/mol |
---|---|
Molecular Formula | Xe |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 0 |
Rotatable Bond Count | 0 |
Exact Mass | 132.90591 g/mol |
Monoisotopic Mass | 132.90591 g/mol |
Topological Polar Surface Area | 0 Ų |
Heavy Atom Count | 1 |
Formal Charge | 0 |
Complexity | 0 |
Isotope Atom Count | 1 |
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 |
1 of 2 | |
---|---|
Drug Name | Xenon xe 133 |
Active Ingredient | Xenon xe-133 |
Dosage Form | Gas |
Route | Inhalation |
Strength | 20mci/vial; 10mci/vial |
Market Status | Prescription |
Company | Lantheus Medcl |
2 of 2 | |
---|---|
Drug Name | Xenon xe 133 |
Active Ingredient | Xenon xe-133 |
Dosage Form | Gas |
Route | Inhalation |
Strength | 20mci/vial; 10mci/vial |
Market Status | Prescription |
Company | Lantheus Medcl |
Inhalation of Xenon Xe 133 Gas has proved valuable for the evaluation of pulmonary function and for imaging the lungs. It may also be applied to assessment of cerebral flow.
Xenon Xe 133 is a readily diffusible gas which is neither utilized nor produced by the body. It passes through cell membranes and freely exchanges between blood and tissue. It tends to concentrate more in body fat than in blood, plasma, water or protein solutions.
V - Various
V09 - Diagnostic radiopharmaceuticals
V09E - Respiratory system
V09EX - Other respiratory system diagnostic radiopharmaceuticals
V09EX03 - Xenon (133Xe) gas
Absorption
Inhaled Xenon Xe 133 Gas will enter the alveolar wall and enter the pulmonary venous circulation via the capillaries.
Route of Elimination
Most of the Xenon Xe 133 that enters the circulation from a single breath is returned to the lungs and exhaled after a single pass through the peripheral circulation.
Half Life 5.245 days
Xenon-133 is used for the diagnostic evaluation of pulmonary function and imaging, as well as assessment of cerebral blood flow. In the concentrations used for diagnostic purposes it is physiologically inactive.
ABOUT THIS PAGE
A Xenon Radioisotopes manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xenon Radioisotopes, including repackagers and relabelers. The FDA regulates Xenon Radioisotopes manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xenon Radioisotopes 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 Xenon Radioisotopes supplier is an individual or a company that provides Xenon Radioisotopes active pharmaceutical ingredient (API) or Xenon Radioisotopes finished formulations upon request. The Xenon Radioisotopes suppliers may include Xenon Radioisotopes API manufacturers, exporters, distributors and traders.
click here to find a list of Xenon Radioisotopes suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Xenon Radioisotopes DMF (Drug Master File) is a document detailing the whole manufacturing process of Xenon Radioisotopes active pharmaceutical ingredient (API) in detail. Different forms of Xenon Radioisotopes DMFs exist exist since differing nations have different regulations, such as Xenon Radioisotopes USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Xenon Radioisotopes DMF submitted to regulatory agencies in the US is known as a USDMF. Xenon Radioisotopes USDMF includes data on Xenon Radioisotopes's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Xenon Radioisotopes USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Xenon Radioisotopes suppliers with USDMF on PharmaCompass.
Xenon Radioisotopes 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 Xenon Radioisotopes 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 Xenon Radioisotopes GMP manufacturer or Xenon Radioisotopes GMP API supplier for your needs.
A Xenon Radioisotopes CoA (Certificate of Analysis) is a formal document that attests to Xenon Radioisotopes's compliance with Xenon Radioisotopes specifications and serves as a tool for batch-level quality control.
Xenon Radioisotopes CoA mostly includes findings from lab analyses of a specific batch. For each Xenon Radioisotopes 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.
Xenon Radioisotopes may be tested according to a variety of international standards, such as European Pharmacopoeia (Xenon Radioisotopes EP), Xenon Radioisotopes JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Xenon Radioisotopes USP).
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