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1. Citicoline Sodium
2. 33818-15-4
3. Citicoline Sodium Salt
4. Cytidine 5'-diphosphocholine Sodium
5. Cdp-choline Sodium
6. Citicoline, Sodium
7. Cdp-choline, Sodium
8. Cytidine 5'-diphosphocholine Sodium Salt
9. Cytidine 5'-diphosphocholine Sodium Salt Dihydrate
10. Cytidine-5'-diphosphocholine Monosodium Salt
11. A821952
12. Sodium [[(2s,3r,4s,5s)-5-(4-amino-2-oxo-pyrimidin-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-oxido-phosphoryl] 2-(trimethylammonio)ethyl Phosphate;citicoline Sodium Salt
| Molecular Weight | 510.31 g/mol |
|---|---|
| Molecular Formula | C14H25N4NaO11P2 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 10 |
| Exact Mass | 510.08927590 g/mol |
| Monoisotopic Mass | 510.08927590 g/mol |
| Topological Polar Surface Area | 216 Ų |
| Heavy Atom Count | 32 |
| Formal Charge | 0 |
| Complexity | 813 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
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PharmaCompass offers a list of Citicoline 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 Citicoline Sodium manufacturer or Citicoline Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Citicoline Sodium manufacturer or Citicoline Sodium supplier.
PharmaCompass also assists you with knowing the Citicoline Sodium API Price utilized in the formulation of products. Citicoline Sodium API Price is not always fixed or binding as the Citicoline Sodium Price is obtained through a variety of data sources. The Citicoline Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CDP-cholin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CDP-cholin, including repackagers and relabelers. The FDA regulates CDP-cholin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CDP-cholin 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 CDP-cholin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CDP-cholin supplier is an individual or a company that provides CDP-cholin active pharmaceutical ingredient (API) or CDP-cholin finished formulations upon request. The CDP-cholin suppliers may include CDP-cholin API manufacturers, exporters, distributors and traders.
click here to find a list of CDP-cholin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CDP-cholin DMF (Drug Master File) is a document detailing the whole manufacturing process of CDP-cholin active pharmaceutical ingredient (API) in detail. Different forms of CDP-cholin DMFs exist exist since differing nations have different regulations, such as CDP-cholin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A CDP-cholin DMF submitted to regulatory agencies in the US is known as a USDMF. CDP-cholin USDMF includes data on CDP-cholin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CDP-cholin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of CDP-cholin suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The CDP-cholin Drug Master File in Japan (CDP-cholin JDMF) empowers CDP-cholin API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the CDP-cholin JDMF during the approval evaluation for pharmaceutical products. At the time of CDP-cholin JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of CDP-cholin suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a CDP-cholin Drug Master File in Korea (CDP-cholin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CDP-cholin. The MFDS reviews the CDP-cholin KDMF as part of the drug registration process and uses the information provided in the CDP-cholin KDMF to evaluate the safety and efficacy of the drug.
After submitting a CDP-cholin KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their CDP-cholin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of CDP-cholin suppliers with KDMF on PharmaCompass.
A CDP-cholin written confirmation (CDP-cholin WC) is an official document issued by a regulatory agency to a CDP-cholin manufacturer, verifying that the manufacturing facility of a CDP-cholin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CDP-cholin APIs or CDP-cholin finished pharmaceutical products to another nation, regulatory agencies frequently require a CDP-cholin WC (written confirmation) as part of the regulatory process.
click here to find a list of CDP-cholin suppliers with Written Confirmation (WC) on PharmaCompass.
CDP-cholin 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 CDP-cholin 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 CDP-cholin GMP manufacturer or CDP-cholin GMP API supplier for your needs.
A CDP-cholin CoA (Certificate of Analysis) is a formal document that attests to CDP-cholin's compliance with CDP-cholin specifications and serves as a tool for batch-level quality control.
CDP-cholin CoA mostly includes findings from lab analyses of a specific batch. For each CDP-cholin 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.
CDP-cholin may be tested according to a variety of international standards, such as European Pharmacopoeia (CDP-cholin EP), CDP-cholin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (CDP-cholin USP).
