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1. Rubidium Chloride Rb 82
2. Rubidium Chloride Rb-82
3. Rubidium Chloride ((sup 82)rbcl)
4. 132486-03-4
5. Rubidium Rb-82 Chloride
6. Rubidium-82(1+);chloride
7. F0z746krkq
8. Rubidium Chloride Rb 82 [usan]
9. Unii-f0z746krkq
10. Rubidium (82rb) Chloride
11. Rubidium Chloride Rb 82 [usan:usp]
12. Ruby-fill
13. Cardiogen-82 (tn)
14. 82rbcl
15. Rubidium (82 Rb) Chloride
16. Chembl1200727
17. Dtxsid60894902
18. Rubidium Chloride Rb 82 (usp)
19. Rubidium (82 Rb) Chloride [who-dd]
20. D05773
21. Rubidium Chloride Rb-82 [orange Book]
22. Q7376097
| Molecular Weight | 117.37 g/mol |
|---|---|
| Molecular Formula | ClRb |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 116.88706 g/mol |
| Monoisotopic Mass | 116.88706 g/mol |
| Topological Polar Surface Area | 0 Ų |
| Heavy Atom Count | 2 |
| Formal Charge | 0 |
| Complexity | 2 |
| 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 | 2 |
Visualisation of myocardial perfusion for diagnostic purposes
Visualisation of myocardial perfusion for diagnostic purposes
V - Various
V09 - Diagnostic radiopharmaceuticals
V09G - Cardiovascular system
V09GX - Other cardiovascular system diagnostic radiopharmaceuticals
V09GX04 - Rubidium (82Rb) chloride
ABOUT THIS PAGE
A Cardiogen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cardiogen, including repackagers and relabelers. The FDA regulates Cardiogen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cardiogen 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 Cardiogen supplier is an individual or a company that provides Cardiogen active pharmaceutical ingredient (API) or Cardiogen finished formulations upon request. The Cardiogen suppliers may include Cardiogen API manufacturers, exporters, distributors and traders.
Cardiogen 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 Cardiogen 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 Cardiogen GMP manufacturer or Cardiogen GMP API supplier for your needs.
A Cardiogen CoA (Certificate of Analysis) is a formal document that attests to Cardiogen's compliance with Cardiogen specifications and serves as a tool for batch-level quality control.
Cardiogen CoA mostly includes findings from lab analyses of a specific batch. For each Cardiogen 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.
Cardiogen may be tested according to a variety of international standards, such as European Pharmacopoeia (Cardiogen EP), Cardiogen JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cardiogen USP).
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