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1. 99m-tc-hmpao
2. 99mtc-hmpao
3. Tc 99m Exametazime
4. Tc 99m Hexamethylpropyleneamine Oxime
5. Tc-99m Hmpao
6. Tc-99m-exametazime
7. Tc-99m-hexamethylpropyleneamine Oxime
8. Technetium Tc 99m Exametazime
9. Technetium Tc 99m Hexamethylpropylene Amine Oxime
10. Technetium Tc 99m Hexamethylpropylene-amine Oxime
11. Technetium Tc 99m Hexamethylpropyleneamine Oxime
1. 99mtc-hida
2. Moli000943
3. 2-[carboxymethyl-[2-(2,6-dimethylanilino)-2-oxoethyl]amino]acetic Acid;technetium-99
| Molecular Weight | 393.21 g/mol |
|---|---|
| Molecular Formula | C14H18N2O5Tc |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 7 |
| Exact Mass | 393.027821 g/mol |
| Monoisotopic Mass | 393.027821 g/mol |
| Topological Polar Surface Area | 107 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 373 |
| Isotope Atom Count | 1 |
| 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 |
| 1 of 1 | |
|---|---|
| Drug Name | Ceretec |
| Active Ingredient | Technetium tc-99m exametazime |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | n/a |
| Market Status | Prescription |
| Company | Ge Healthcare |
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.)
ABOUT THIS PAGE
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PharmaCompass offers a list of Ceretec 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 Ceretec manufacturer or Ceretec supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ceretec manufacturer or Ceretec supplier.
PharmaCompass also assists you with knowing the Ceretec API Price utilized in the formulation of products. Ceretec API Price is not always fixed or binding as the Ceretec Price is obtained through a variety of data sources. The Ceretec Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ceretec manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ceretec, including repackagers and relabelers. The FDA regulates Ceretec manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ceretec 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 Ceretec supplier is an individual or a company that provides Ceretec active pharmaceutical ingredient (API) or Ceretec finished formulations upon request. The Ceretec suppliers may include Ceretec API manufacturers, exporters, distributors and traders.
Ceretec 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 Ceretec 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 Ceretec GMP manufacturer or Ceretec GMP API supplier for your needs.
A Ceretec CoA (Certificate of Analysis) is a formal document that attests to Ceretec's compliance with Ceretec specifications and serves as a tool for batch-level quality control.
Ceretec CoA mostly includes findings from lab analyses of a specific batch. For each Ceretec 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.
Ceretec may be tested according to a variety of international standards, such as European Pharmacopoeia (Ceretec EP), Ceretec JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ceretec USP).
