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1. Iron(iii)choline Citrate
| Molecular Weight | 997.5 g/mol |
|---|---|
| Molecular Formula | C33H63Fe2N3O24 |
| Hydrogen Bond Donor Count | 12 |
| Hydrogen Bond Acceptor Count | 24 |
| Rotatable Bond Count | 12 |
| Exact Mass | 997.250021 g/mol |
| Monoisotopic Mass | 997.250021 g/mol |
| Topological Polar Surface Area | 466 Ų |
| Heavy Atom Count | 62 |
| Formal Charge | 0 |
| Complexity | 955 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 8 |
ABOUT THIS PAGE
A Iron(III) Choline Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iron(III) Choline Citrate, including repackagers and relabelers. The FDA regulates Iron(III) Choline Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iron(III) Choline Citrate 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 Iron(III) Choline Citrate supplier is an individual or a company that provides Iron(III) Choline Citrate active pharmaceutical ingredient (API) or Iron(III) Choline Citrate finished formulations upon request. The Iron(III) Choline Citrate suppliers may include Iron(III) Choline Citrate API manufacturers, exporters, distributors and traders.
Iron(III) Choline Citrate 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 Iron(III) Choline Citrate 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 Iron(III) Choline Citrate GMP manufacturer or Iron(III) Choline Citrate GMP API supplier for your needs.
A Iron(III) Choline Citrate CoA (Certificate of Analysis) is a formal document that attests to Iron(III) Choline Citrate's compliance with Iron(III) Choline Citrate specifications and serves as a tool for batch-level quality control.
Iron(III) Choline Citrate CoA mostly includes findings from lab analyses of a specific batch. For each Iron(III) Choline Citrate 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.
Iron(III) Choline Citrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Iron(III) Choline Citrate EP), Iron(III) Choline Citrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Iron(III) Choline Citrate USP).
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