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1. Neridronate Sodium
2. Neridronate Sodium Salt
3. 80729-79-9
4. Neridronate Monosodium
5. H6jvb49q0f
6. Neridronate, Sodium Salt
7. (6-amino-1-hydroxyhexylidene)bisphosphonic Acid, Sodium Salt
8. Sodium;(6-amino-1-hydroxy-1-phosphonohexyl)-hydroxyphosphinate
9. Sodium Hydrogen (6-amino-1-hydroxy-1-phosphonohexyl)phosphonate
10. Unii-h6jvb49q0f
11. Schembl328774
12. Neridronate Sodium [mart.]
13. Neridronate Sodium [who-dd]
14. Neridronic Acid Monosodium Salt
15. Ft-0672683
16. Neridronic Acid Monosodium Salt [mi]
17. Q27279709
| Molecular Weight | 299.13 g/mol |
|---|---|
| Molecular Formula | C6H16NNaO7P2 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 7 |
| Exact Mass | 299.02997013 g/mol |
| Monoisotopic Mass | 299.02997013 g/mol |
| Topological Polar Surface Area | 164 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 322 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
Market Place
FDF DOSSIERS
Reply
24 May 2017
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ABOUT THIS PAGE
18
PharmaCompass offers a list of Neridronate Sodium 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 Neridronate Sodium manufacturer or Neridronate Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Neridronate Sodium manufacturer or Neridronate Sodium supplier.
PharmaCompass also assists you with knowing the Neridronate Sodium API Price utilized in the formulation of products. Neridronate Sodium API Price is not always fixed or binding as the Neridronate Sodium Price is obtained through a variety of data sources. The Neridronate Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nerixia manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nerixia, including repackagers and relabelers. The FDA regulates Nerixia manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nerixia 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 Nerixia supplier is an individual or a company that provides Nerixia active pharmaceutical ingredient (API) or Nerixia finished formulations upon request. The Nerixia suppliers may include Nerixia API manufacturers, exporters, distributors and traders.
Nerixia 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 Nerixia 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 Nerixia GMP manufacturer or Nerixia GMP API supplier for your needs.
A Nerixia CoA (Certificate of Analysis) is a formal document that attests to Nerixia's compliance with Nerixia specifications and serves as a tool for batch-level quality control.
Nerixia CoA mostly includes findings from lab analyses of a specific batch. For each Nerixia 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.
Nerixia may be tested according to a variety of international standards, such as European Pharmacopoeia (Nerixia EP), Nerixia JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Nerixia USP).
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