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1. Choline Citrate (1:1)
2. 2-(carboxymethyl)-2,4-dihydroxy-4-oxobutanoate;2-hydroxyethyl(trimethyl)azanium
3. Cirrocolina
4. Citracholin
5. Citracholine
6. Citrocholine
7. Colicitrin
8. Neurotropan
9. Cholinvel
10. Citrocol
11. Delichol
12. Cholex
13. Ethanaminium, 2-hydroxy-n,n,n-trimethyl-, 2-hydroxy-1,2,3-propanetricarboxylate (1:1)
14. Einecs 201-068-6
15. Choline Hydrogencitrate
16. Unii-dq8hhp07gl
17. Choline Dihydrogen Citrate (tn)
18. Choline Dihydrogen Citrate [nf]
19. Schembl16267377
20. Dtxsid30889325
21. Ls-14019
22. Salts Of (2-hydroxyethyl)trimethylammonium
23. D07691
24. 4-amino-4-(2-carboxyethyl)-heptanedioicacid
Molecular Weight | 295.29 g/mol |
---|---|
Molecular Formula | C11H21NO8 |
Hydrogen Bond Donor Count | 4 |
Hydrogen Bond Acceptor Count | 8 |
Rotatable Bond Count | 6 |
Exact Mass | 295.12671663 g/mol |
Monoisotopic Mass | 295.12671663 g/mol |
Topological Polar Surface Area | 155 Ų |
Heavy Atom Count | 20 |
Formal Charge | 0 |
Complexity | 268 |
Isotope Atom Count | 0 |
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 |
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ABOUT THIS PAGE
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PharmaCompass offers a list of Choline Dihydrogen Citrate 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 Choline Dihydrogen Citrate manufacturer or Choline Dihydrogen Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Choline Dihydrogen Citrate manufacturer or Choline Dihydrogen Citrate supplier.
PharmaCompass also assists you with knowing the Choline Dihydrogen Citrate API Price utilized in the formulation of products. Choline Dihydrogen Citrate API Price is not always fixed or binding as the Choline Dihydrogen Citrate Price is obtained through a variety of data sources. The Choline Dihydrogen Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neurotropan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neurotropan, including repackagers and relabelers. The FDA regulates Neurotropan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neurotropan API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Neurotropan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Neurotropan supplier is an individual or a company that provides Neurotropan active pharmaceutical ingredient (API) or Neurotropan finished formulations upon request. The Neurotropan suppliers may include Neurotropan API manufacturers, exporters, distributors and traders.
click here to find a list of Neurotropan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Neurotropan written confirmation (Neurotropan WC) is an official document issued by a regulatory agency to a Neurotropan manufacturer, verifying that the manufacturing facility of a Neurotropan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Neurotropan APIs or Neurotropan finished pharmaceutical products to another nation, regulatory agencies frequently require a Neurotropan WC (written confirmation) as part of the regulatory process.
click here to find a list of Neurotropan suppliers with Written Confirmation (WC) on PharmaCompass.
Neurotropan 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 Neurotropan 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 Neurotropan GMP manufacturer or Neurotropan GMP API supplier for your needs.
A Neurotropan CoA (Certificate of Analysis) is a formal document that attests to Neurotropan's compliance with Neurotropan specifications and serves as a tool for batch-level quality control.
Neurotropan CoA mostly includes findings from lab analyses of a specific batch. For each Neurotropan 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.
Neurotropan may be tested according to a variety of international standards, such as European Pharmacopoeia (Neurotropan EP), Neurotropan JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Neurotropan USP).