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1. 99mtc-tetrafosmin
2. 99mtc-tetrofosmin
3. Myoview
4. Ppn-1011
5. Ppn1011
6. Tc-99m-ppn1011
7. Tc-99m-tetrofosmin
8. Technetium Tc 99m 1,2-bis(bis(2-ethoxyethyl)phosphino)ethane
9. Technetium Tc-99m Tetrofosmin
10. Technetium(1+)-99tc, Bis(6,9-bis(2-ethoxyethyl)-3,12-dioxa-6,9-diphosphatetradecane-.kappa.p,.kappa.p')dioxo-, (oc-6-11)-
11. Technetium-99m-tetrofosmin
1. Technetium Tc-99m Tetrofosmin
2. Q7692231
Molecular Weight | 479.4 g/mol |
---|---|
Molecular Formula | C18H40O4P2Tc |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 19 |
Exact Mass | 479.14654 g/mol |
Monoisotopic Mass | 479.14654 g/mol |
Topological Polar Surface Area | 36.9 Ų |
Heavy Atom Count | 25 |
Formal Charge | 0 |
Complexity | 201 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
Radiopharmaceuticals
Compounds that are used in medicine as sources of radiation for radiotherapy and for diagnostic purposes. They have numerous uses in research and industry. (Martindale, The Extra Pharmacopoeia, 30th ed, p1161) (See all compounds classified as Radiopharmaceuticals.)
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PharmaCompass offers a list of Tc-99M Tetrofosmin 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 Tc-99M Tetrofosmin manufacturer or Tc-99M Tetrofosmin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tc-99M Tetrofosmin manufacturer or Tc-99M Tetrofosmin supplier.
PharmaCompass also assists you with knowing the Tc-99M Tetrofosmin API Price utilized in the formulation of products. Tc-99M Tetrofosmin API Price is not always fixed or binding as the Tc-99M Tetrofosmin Price is obtained through a variety of data sources. The Tc-99M Tetrofosmin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MYOVIEW 30ML manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MYOVIEW 30ML, including repackagers and relabelers. The FDA regulates MYOVIEW 30ML manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MYOVIEW 30ML 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 MYOVIEW 30ML supplier is an individual or a company that provides MYOVIEW 30ML active pharmaceutical ingredient (API) or MYOVIEW 30ML finished formulations upon request. The MYOVIEW 30ML suppliers may include MYOVIEW 30ML API manufacturers, exporters, distributors and traders.
MYOVIEW 30ML 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 MYOVIEW 30ML 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 MYOVIEW 30ML GMP manufacturer or MYOVIEW 30ML GMP API supplier for your needs.
A MYOVIEW 30ML CoA (Certificate of Analysis) is a formal document that attests to MYOVIEW 30ML's compliance with MYOVIEW 30ML specifications and serves as a tool for batch-level quality control.
MYOVIEW 30ML CoA mostly includes findings from lab analyses of a specific batch. For each MYOVIEW 30ML 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.
MYOVIEW 30ML may be tested according to a variety of international standards, such as European Pharmacopoeia (MYOVIEW 30ML EP), MYOVIEW 30ML JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MYOVIEW 30ML USP).