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1. Aldoxorubicin Hydrochloride
2. Hy-16261b
3. Cs-0077171
4. Q27288392
Molecular Weight | 787.2 g/mol |
---|---|
Molecular Formula | C37H43ClN4O13 |
Hydrogen Bond Donor Count | 8 |
Hydrogen Bond Acceptor Count | 15 |
Rotatable Bond Count | 12 |
Exact Mass | 786.2515151 g/mol |
Monoisotopic Mass | 786.2515151 g/mol |
Topological Polar Surface Area | 268 Ų |
Heavy Atom Count | 55 |
Formal Charge | 0 |
Complexity | 1510 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 6 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 1 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
A Aldoxorubicin HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aldoxorubicin HCl, including repackagers and relabelers. The FDA regulates Aldoxorubicin HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aldoxorubicin HCl 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 Aldoxorubicin HCl supplier is an individual or a company that provides Aldoxorubicin HCl active pharmaceutical ingredient (API) or Aldoxorubicin HCl finished formulations upon request. The Aldoxorubicin HCl suppliers may include Aldoxorubicin HCl API manufacturers, exporters, distributors and traders.
Aldoxorubicin HCl 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 Aldoxorubicin HCl 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 Aldoxorubicin HCl GMP manufacturer or Aldoxorubicin HCl GMP API supplier for your needs.
A Aldoxorubicin HCl CoA (Certificate of Analysis) is a formal document that attests to Aldoxorubicin HCl's compliance with Aldoxorubicin HCl specifications and serves as a tool for batch-level quality control.
Aldoxorubicin HCl CoA mostly includes findings from lab analyses of a specific batch. For each Aldoxorubicin HCl 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.
Aldoxorubicin HCl may be tested according to a variety of international standards, such as European Pharmacopoeia (Aldoxorubicin HCl EP), Aldoxorubicin HCl JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Aldoxorubicin HCl USP).
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