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| Molecular Weight | 517.4 g/mol |
|---|---|
| Molecular Formula | C20H21N7Na2O7 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 7 |
| Exact Mass | 517.12978460 g/mol |
| Monoisotopic Mass | 517.12978460 g/mol |
| Topological Polar Surface Area | 221 A^2 |
| Heavy Atom Count | 36 |
| Formal Charge | 0 |
| Complexity | 900 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 3 |
Market Place
ABOUT THIS PAGE
A Disodium Folinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disodium Folinate, including repackagers and relabelers. The FDA regulates Disodium Folinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disodium Folinate 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 Disodium Folinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Disodium Folinate supplier is an individual or a company that provides Disodium Folinate active pharmaceutical ingredient (API) or Disodium Folinate finished formulations upon request. The Disodium Folinate suppliers may include Disodium Folinate API manufacturers, exporters, distributors and traders.
click here to find a list of Disodium Folinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Disodium Folinate 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 Disodium Folinate 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 Disodium Folinate GMP manufacturer or Disodium Folinate GMP API supplier for your needs.
A Disodium Folinate CoA (Certificate of Analysis) is a formal document that attests to Disodium Folinate's compliance with Disodium Folinate specifications and serves as a tool for batch-level quality control.
Disodium Folinate CoA mostly includes findings from lab analyses of a specific batch. For each Disodium Folinate 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.
Disodium Folinate may be tested according to a variety of international standards, such as European Pharmacopoeia (Disodium Folinate EP), Disodium Folinate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Disodium Folinate USP).
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