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1. Fw5vy7926x
2. 1-cyclopentene-1-carboxylic Acid, 2-(((3-fluoro-3'-methoxy(1,1'-biphenyl)-4-yl)amino)carbonyl)-, Calcium Salt (2:1)
3. 1354012-90-0
4. Unii-fw5vy7926x
5. Vidofludimus Calcium [who-dd]
Molecular Weight | 748.8 g/mol |
---|---|
Molecular Formula | C40H34CaF2N2O8 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 10 |
Rotatable Bond Count | 8 |
Exact Mass | 748.1909132 g/mol |
Monoisotopic Mass | 748.1909132 g/mol |
Topological Polar Surface Area | 157 Ų |
Heavy Atom Count | 53 |
Formal Charge | 0 |
Complexity | 571 |
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 | 3 |
ABOUT THIS PAGE
A Vidofludimus Calcium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vidofludimus Calcium, including repackagers and relabelers. The FDA regulates Vidofludimus Calcium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vidofludimus Calcium 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 Vidofludimus Calcium supplier is an individual or a company that provides Vidofludimus Calcium active pharmaceutical ingredient (API) or Vidofludimus Calcium finished formulations upon request. The Vidofludimus Calcium suppliers may include Vidofludimus Calcium API manufacturers, exporters, distributors and traders.
Vidofludimus Calcium 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 Vidofludimus Calcium 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 Vidofludimus Calcium GMP manufacturer or Vidofludimus Calcium GMP API supplier for your needs.
A Vidofludimus Calcium CoA (Certificate of Analysis) is a formal document that attests to Vidofludimus Calcium's compliance with Vidofludimus Calcium specifications and serves as a tool for batch-level quality control.
Vidofludimus Calcium CoA mostly includes findings from lab analyses of a specific batch. For each Vidofludimus Calcium 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.
Vidofludimus Calcium may be tested according to a variety of international standards, such as European Pharmacopoeia (Vidofludimus Calcium EP), Vidofludimus Calcium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vidofludimus Calcium USP).
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