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1. 127xe Radioisotope
2. Xe-127 Radioisotope
3. Xenon-127
1. Xenon-127
2. Xenon Xe 127
3. 13994-19-9
4. Xenon, Isotope Of Mass 127
5. Xenon 127
6. Xenon, Xe-127
7. Xenon (127xe)
8. H95kbr1gdb
9. Xenon Xe 127 [usp]
10. Xenon Xe 127 (usp)
11. Xenon (127xe) Gas
12. Unii-h95kbr1gdb
13. Xenon Xe 127 (tn)
14. Chembl1200673
15. Xenon-127 [mart.]
16. Dtxsid10930667
17. 127xe
18. Moli000992
19. Xenon Xe-127 [orange Book]
20. Db09461
21. Xenon Xe 127 [usp Impurity]
22. D06338
23. Q2304361
| Molecular Weight | 126.90518 g/mol |
|---|---|
| Molecular Formula | Xe |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 126.90518 g/mol |
| Monoisotopic Mass | 126.90518 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 |
V - Various
V09 - Diagnostic radiopharmaceuticals
V09E - Respiratory system
V09EX - Other respiratory system diagnostic radiopharmaceuticals
V09EX02 - Xenon (127Xe) gas
ABOUT THIS PAGE
A Xenon 127 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xenon 127, including repackagers and relabelers. The FDA regulates Xenon 127 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xenon 127 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 127 supplier is an individual or a company that provides Xenon 127 active pharmaceutical ingredient (API) or Xenon 127 finished formulations upon request. The Xenon 127 suppliers may include Xenon 127 API manufacturers, exporters, distributors and traders.
click here to find a list of Xenon 127 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Xenon 127 DMF (Drug Master File) is a document detailing the whole manufacturing process of Xenon 127 active pharmaceutical ingredient (API) in detail. Different forms of Xenon 127 DMFs exist exist since differing nations have different regulations, such as Xenon 127 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Xenon 127 DMF submitted to regulatory agencies in the US is known as a USDMF. Xenon 127 USDMF includes data on Xenon 127's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Xenon 127 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Xenon 127 suppliers with USDMF on PharmaCompass.
Xenon 127 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 127 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 127 GMP manufacturer or Xenon 127 GMP API supplier for your needs.
A Xenon 127 CoA (Certificate of Analysis) is a formal document that attests to Xenon 127's compliance with Xenon 127 specifications and serves as a tool for batch-level quality control.
Xenon 127 CoA mostly includes findings from lab analyses of a specific batch. For each Xenon 127 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 127 may be tested according to a variety of international standards, such as European Pharmacopoeia (Xenon 127 EP), Xenon 127 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Xenon 127 USP).
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