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1. 56254-07-0
2. Iodohippurate Sodium I-123
3. Iodohippurate I123 Sodium
4. Iodohippurate Sodium,i-123
5. 4nw20gfq7h
6. Iodohippurate Sodium, I-123
7. Sodium Iodohippurate (123 I)
8. Sodium Iodohippurate (123-i)
9. Sodium;2-[(2-(123i)iodanylbenzoyl)amino]acetate
10. Nephroflow
11. 123i-iodohippuran
12. Hippuran-123i
13. Unii-4nw20gfq7h
14. Nephroflow (tn)
15. Iodohippurate Sodium I 123 [usan]
16. Sodium O-iodo-(sup 123)i-hippurate
17. Iodohippurate Sodium I 123 [usan:usp]
18. Sodium Iodohippurate (123i)
19. Sodium O-iodo-123i-hippurate
20. Chembl1200439
21. Dtxsid60204805
22. Iodohippurate Sodium I 123 (usp)
23. Iodohippurate Sodium,i-123 [vandf]
24. D04568
25. O-iodohippurate Sodium 123i-labeled Form
26. Sodium Iodohippurate (123 I) [who-dd]
27. Iodohippurate Sodium I 123 [usp Impurity]
28. Iodohippurate Sodium I-123 [orange Book]
29. O-iodohippurate Sodium 123i-labeled Form [mi]
30. Q27260255
31. Glycine, N-(2-(iodo-(sup 123)i)benzoyl)-, Monosodium Salt
32. Glycine, N-(2-(iodo-(sup 123)i) Benzoyl)-, Monosodium Salt
| Molecular Weight | 323.05 g/mol |
|---|---|
| Molecular Formula | C9H7INNaO3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 3 |
| Exact Mass | 322.93795 g/mol |
| Monoisotopic Mass | 322.93795 g/mol |
| Topological Polar Surface Area | 69.2 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 237 |
| 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 |
V - Various
V09 - Diagnostic radiopharmaceuticals
V09C - Renal system
V09CX - Other renal system diagnostic radiopharmaceuticals
V09CX01 - Sodium iodohippurate (123I)
ABOUT THIS PAGE
11
PharmaCompass offers a list of Nephroflow API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Nephroflow manufacturer or Nephroflow supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nephroflow manufacturer or Nephroflow supplier.
PharmaCompass also assists you with knowing the Nephroflow API Price utilized in the formulation of products. Nephroflow API Price is not always fixed or binding as the Nephroflow Price is obtained through a variety of data sources. The Nephroflow Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nephroflow manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nephroflow, including repackagers and relabelers. The FDA regulates Nephroflow manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nephroflow 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 Nephroflow supplier is an individual or a company that provides Nephroflow active pharmaceutical ingredient (API) or Nephroflow finished formulations upon request. The Nephroflow suppliers may include Nephroflow API manufacturers, exporters, distributors and traders.
Nephroflow 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 Nephroflow 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 Nephroflow GMP manufacturer or Nephroflow GMP API supplier for your needs.
A Nephroflow CoA (Certificate of Analysis) is a formal document that attests to Nephroflow's compliance with Nephroflow specifications and serves as a tool for batch-level quality control.
Nephroflow CoA mostly includes findings from lab analyses of a specific batch. For each Nephroflow 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.
Nephroflow may be tested according to a variety of international standards, such as European Pharmacopoeia (Nephroflow EP), Nephroflow JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Nephroflow USP).
