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| Molecular Weight | 458.5 g/mol |
|---|---|
| Molecular Formula | C21H22N4O6S |
| XLogP3 | 1.4 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 9 |
| Exact Mass | 458.12600561 g/mol |
| Monoisotopic Mass | 458.12600561 g/mol |
| Topological Polar Surface Area | 177 A^2 |
| Heavy Atom Count | 32 |
| Formal Charge | 0 |
| Complexity | 790 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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A Raltitrexed manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Raltitrexed, including repackagers and relabelers. The FDA regulates Raltitrexed manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Raltitrexed 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 Raltitrexed manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Raltitrexed supplier is an individual or a company that provides Raltitrexed active pharmaceutical ingredient (API) or Raltitrexed finished formulations upon request. The Raltitrexed suppliers may include Raltitrexed API manufacturers, exporters, distributors and traders.
click here to find a list of Raltitrexed suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Raltitrexed 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 Raltitrexed 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 Raltitrexed GMP manufacturer or Raltitrexed GMP API supplier for your needs.
A Raltitrexed CoA (Certificate of Analysis) is a formal document that attests to Raltitrexed's compliance with Raltitrexed specifications and serves as a tool for batch-level quality control.
Raltitrexed CoA mostly includes findings from lab analyses of a specific batch. For each Raltitrexed 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.
Raltitrexed may be tested according to a variety of international standards, such as European Pharmacopoeia (Raltitrexed EP), Raltitrexed JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Raltitrexed USP).
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