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1. Wustite
1. Iron(ii) Oxide
2. Oxoiron
3. 1345-25-1
4. Iron Monooxide
5. Iron Monoxide
6. Iron(ii)oxide
7. Wustite
8. Natural Wuestite
9. Eisenoxydul
10. Iron-oxygen
11. Unii-g7036x8b5h
12. Hsdb 464
13. Eisen(ii)-oxid
14. Iron(2) Oxide
15. Einecs 215-721-8
16. Iron(2+) Oxide
17. Iron(ii) Oxide, Cp
18. Ec 215-721-8
19. Iron(2+);oxygen(2-)
20. Chebi:50820
21. Mfcd00016095
22. Akos015913785
23. 17125-56-3
24. Q196680
25. Iron(ii) Oxide, -10 Mesh, 99.8% Trace Metals Basis
| Molecular Weight | 71.84 g/mol |
|---|---|
| Molecular Formula | FeO |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 71.929850 g/mol |
| Monoisotopic Mass | 71.929850 g/mol |
| Topological Polar Surface Area | 17.1 Ų |
| Heavy Atom Count | 2 |
| Formal Charge | 0 |
| Complexity | 2 |
| 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 | 1 |
API SUPPLIERS
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ABOUT THIS PAGE
A Iron monooxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iron monooxide, including repackagers and relabelers. The FDA regulates Iron monooxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iron monooxide 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 monooxide supplier is an individual or a company that provides Iron monooxide active pharmaceutical ingredient (API) or Iron monooxide finished formulations upon request. The Iron monooxide suppliers may include Iron monooxide API manufacturers, exporters, distributors and traders.
click here to find a list of Iron monooxide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Iron monooxide DMF (Drug Master File) is a document detailing the whole manufacturing process of Iron monooxide active pharmaceutical ingredient (API) in detail. Different forms of Iron monooxide DMFs exist exist since differing nations have different regulations, such as Iron monooxide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Iron monooxide DMF submitted to regulatory agencies in the US is known as a USDMF. Iron monooxide USDMF includes data on Iron monooxide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Iron monooxide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Iron monooxide suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Iron monooxide Drug Master File in Japan (Iron monooxide JDMF) empowers Iron monooxide API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Iron monooxide JDMF during the approval evaluation for pharmaceutical products. At the time of Iron monooxide JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Iron monooxide suppliers with JDMF on PharmaCompass.
Iron monooxide 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 monooxide 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 monooxide GMP manufacturer or Iron monooxide GMP API supplier for your needs.
A Iron monooxide CoA (Certificate of Analysis) is a formal document that attests to Iron monooxide's compliance with Iron monooxide specifications and serves as a tool for batch-level quality control.
Iron monooxide CoA mostly includes findings from lab analyses of a specific batch. For each Iron monooxide 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 monooxide may be tested according to a variety of international standards, such as European Pharmacopoeia (Iron monooxide EP), Iron monooxide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Iron monooxide USP).
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