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1. 177lu-dota-hh1
2. 177lu-tetraxetan-tetulomab
3. 177lu-tetulomab
4. Tetulomab Tetraxetan Lu-177
1. Tetulomab Tetraxetan Lu-177
2. 6qu69vig75
3. Db12227
4. Lysine .episilon.carbamothiobenzyl-2-tetraxan
| Molecular Weight | 697.8 g/mol |
|---|---|
| Molecular Formula | C30H47N7O10S |
| XLogP3 | -11.5 |
| Hydrogen Bond Donor Count | 8 |
| Hydrogen Bond Acceptor Count | 16 |
| Rotatable Bond Count | 17 |
| Exact Mass | 697.31051190 g/mol |
| Monoisotopic Mass | 697.31051190 g/mol |
| Topological Polar Surface Area | 282 Ų |
| Heavy Atom Count | 48 |
| Formal Charge | 0 |
| Complexity | 1080 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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PharmaCompass offers a list of Tetulomab Tetraxetan Lu-177 API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Tetulomab Tetraxetan Lu-177 manufacturer or Tetulomab Tetraxetan Lu-177 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tetulomab Tetraxetan Lu-177 manufacturer or Tetulomab Tetraxetan Lu-177 supplier.
PharmaCompass also assists you with knowing the Tetulomab Tetraxetan Lu-177 API Price utilized in the formulation of products. Tetulomab Tetraxetan Lu-177 API Price is not always fixed or binding as the Tetulomab Tetraxetan Lu-177 Price is obtained through a variety of data sources. The Tetulomab Tetraxetan Lu-177 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tetulomab Tetraxetan Lu-177 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetulomab Tetraxetan Lu-177, including repackagers and relabelers. The FDA regulates Tetulomab Tetraxetan Lu-177 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetulomab Tetraxetan Lu-177 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 Tetulomab Tetraxetan Lu-177 supplier is an individual or a company that provides Tetulomab Tetraxetan Lu-177 active pharmaceutical ingredient (API) or Tetulomab Tetraxetan Lu-177 finished formulations upon request. The Tetulomab Tetraxetan Lu-177 suppliers may include Tetulomab Tetraxetan Lu-177 API manufacturers, exporters, distributors and traders.
Tetulomab Tetraxetan Lu-177 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 Tetulomab Tetraxetan Lu-177 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 Tetulomab Tetraxetan Lu-177 GMP manufacturer or Tetulomab Tetraxetan Lu-177 GMP API supplier for your needs.
A Tetulomab Tetraxetan Lu-177 CoA (Certificate of Analysis) is a formal document that attests to Tetulomab Tetraxetan Lu-177's compliance with Tetulomab Tetraxetan Lu-177 specifications and serves as a tool for batch-level quality control.
Tetulomab Tetraxetan Lu-177 CoA mostly includes findings from lab analyses of a specific batch. For each Tetulomab Tetraxetan Lu-177 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.
Tetulomab Tetraxetan Lu-177 may be tested according to a variety of international standards, such as European Pharmacopoeia (Tetulomab Tetraxetan Lu-177 EP), Tetulomab Tetraxetan Lu-177 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tetulomab Tetraxetan Lu-177 USP).
