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| Molecular Weight | 487.5 g/mol |
|---|---|
| Molecular Formula | C24H22FNO7S-2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 6 |
| Exact Mass | 487.11010138 g/mol |
| Monoisotopic Mass | 487.11010138 g/mol |
| Topological Polar Surface Area | 155 Ų |
| Heavy Atom Count | 34 |
| Formal Charge | -2 |
| Complexity | 663 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
A Prasugrel Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prasugrel Maleate, including repackagers and relabelers. The FDA regulates Prasugrel Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prasugrel Maleate 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 Prasugrel Maleate supplier is an individual or a company that provides Prasugrel Maleate active pharmaceutical ingredient (API) or Prasugrel Maleate finished formulations upon request. The Prasugrel Maleate suppliers may include Prasugrel Maleate API manufacturers, exporters, distributors and traders.
Prasugrel Maleate 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 Prasugrel Maleate 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 Prasugrel Maleate GMP manufacturer or Prasugrel Maleate GMP API supplier for your needs.
A Prasugrel Maleate CoA (Certificate of Analysis) is a formal document that attests to Prasugrel Maleate's compliance with Prasugrel Maleate specifications and serves as a tool for batch-level quality control.
Prasugrel Maleate CoA mostly includes findings from lab analyses of a specific batch. For each Prasugrel Maleate 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.
Prasugrel Maleate may be tested according to a variety of international standards, such as European Pharmacopoeia (Prasugrel Maleate EP), Prasugrel Maleate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Prasugrel Maleate USP).
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