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1. 57680-55-4
2. Gleptoferronum
3. Gleptosil
4. Heptomer
5. Gleptoferronum [inn-latin]
6. Unii-898723iqhq
7. Gleptoferron [usan:inn:ban]
8. 898723iqhq
| Molecular Weight | 477.17 g/mol |
|---|---|
| Molecular Formula | C13H25FeO15- |
| Hydrogen Bond Donor Count | 11 |
| Hydrogen Bond Acceptor Count | 15 |
| Rotatable Bond Count | 9 |
| Exact Mass | 477.054281 g/mol |
| Monoisotopic Mass | 477.054281 g/mol |
| Topological Polar Surface Area | 281 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | -1 |
| Complexity | 448 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 5 |
| Undefined Atom Stereocenter Count | 5 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 3 |
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24 Jun 2023
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06 Nov 2021
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ABOUT THIS PAGE
A UNII-898723IQHQ manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UNII-898723IQHQ, including repackagers and relabelers. The FDA regulates UNII-898723IQHQ manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UNII-898723IQHQ 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 UNII-898723IQHQ supplier is an individual or a company that provides UNII-898723IQHQ active pharmaceutical ingredient (API) or UNII-898723IQHQ finished formulations upon request. The UNII-898723IQHQ suppliers may include UNII-898723IQHQ API manufacturers, exporters, distributors and traders.
UNII-898723IQHQ 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 UNII-898723IQHQ 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 UNII-898723IQHQ GMP manufacturer or UNII-898723IQHQ GMP API supplier for your needs.
A UNII-898723IQHQ CoA (Certificate of Analysis) is a formal document that attests to UNII-898723IQHQ's compliance with UNII-898723IQHQ specifications and serves as a tool for batch-level quality control.
UNII-898723IQHQ CoA mostly includes findings from lab analyses of a specific batch. For each UNII-898723IQHQ 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.
UNII-898723IQHQ may be tested according to a variety of international standards, such as European Pharmacopoeia (UNII-898723IQHQ EP), UNII-898723IQHQ JP (Japanese Pharmacopeia) and the US Pharmacopoeia (UNII-898723IQHQ USP).
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