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1. Aldoxorubicin
2. Doxo-emch
3. Inno-206
1. Doxo-emch
2. Inno-206
3. Aldoxorubicin
4. C28mv4im0b
5. 151038-96-9
6. Unii-c28mv4im0b
7. Aldoxorubicin [usan:inn]
8. Inno 206
9. Dtxsid301318641
10. 1361644-26-9
Molecular Weight | 750.7 g/mol |
---|---|
Molecular Formula | C37H42N4O13 |
XLogP3 | 1.3 |
Hydrogen Bond Donor Count | 7 |
Hydrogen Bond Acceptor Count | 15 |
Rotatable Bond Count | 12 |
Exact Mass | 750.27483741 g/mol |
Monoisotopic Mass | 750.27483741 g/mol |
Topological Polar Surface Area | 268 Ų |
Heavy Atom Count | 54 |
Formal Charge | 0 |
Complexity | 1510 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 6 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 1 |
Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A D00CZL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of D00CZL, including repackagers and relabelers. The FDA regulates D00CZL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. D00CZL 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 D00CZL supplier is an individual or a company that provides D00CZL active pharmaceutical ingredient (API) or D00CZL finished formulations upon request. The D00CZL suppliers may include D00CZL API manufacturers, exporters, distributors and traders.
D00CZL 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 D00CZL 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 D00CZL GMP manufacturer or D00CZL GMP API supplier for your needs.
A D00CZL CoA (Certificate of Analysis) is a formal document that attests to D00CZL's compliance with D00CZL specifications and serves as a tool for batch-level quality control.
D00CZL CoA mostly includes findings from lab analyses of a specific batch. For each D00CZL 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.
D00CZL may be tested according to a variety of international standards, such as European Pharmacopoeia (D00CZL EP), D00CZL JP (Japanese Pharmacopeia) and the US Pharmacopoeia (D00CZL USP).
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