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1. Fe3(po4)2.8h2o
2. Vivianite
1. 14940-41-1
2. Iron(ii) Phosphate
3. Iron(2+);diphosphate
4. Triiron Bis(orthophosphate)
5. Phosphoric Acid, Iron(2+) Salt (2:3)
6. Iron(ii) Orthophosphate
7. D07l04mrwi
8. Ferrophosphate
9. Unii-d07l04mrwi
10. Einecs 239-018-0
11. Iron (ii) Phosphate
12. Ferrous Orthophosphate
13. Ferrous Phosphate [mi]
14. Dtxsid20872569
15. Ferrous Phosphate [who-dd]
16. Iron Phosphate (fe3(po4)2)
17. Q2618789
Molecular Weight | 357.48 g/mol |
---|---|
Molecular Formula | Fe3O8P2 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 8 |
Rotatable Bond Count | 0 |
Exact Mass | 357.711648 g/mol |
Monoisotopic Mass | 357.711648 g/mol |
Topological Polar Surface Area | 173 Ų |
Heavy Atom Count | 13 |
Formal Charge | 0 |
Complexity | 36.8 |
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 | 5 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Ferrous phosphate 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 Ferrous phosphate manufacturer or Ferrous phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ferrous phosphate manufacturer or Ferrous phosphate supplier.
PharmaCompass also assists you with knowing the Ferrous phosphate API Price utilized in the formulation of products. Ferrous phosphate API Price is not always fixed or binding as the Ferrous phosphate Price is obtained through a variety of data sources. The Ferrous phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Iron (II) Phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iron (II) Phosphate, including repackagers and relabelers. The FDA regulates Iron (II) Phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iron (II) Phosphate 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 (II) Phosphate supplier is an individual or a company that provides Iron (II) Phosphate active pharmaceutical ingredient (API) or Iron (II) Phosphate finished formulations upon request. The Iron (II) Phosphate suppliers may include Iron (II) Phosphate API manufacturers, exporters, distributors and traders.
Iron (II) Phosphate 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 (II) Phosphate 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 (II) Phosphate GMP manufacturer or Iron (II) Phosphate GMP API supplier for your needs.
A Iron (II) Phosphate CoA (Certificate of Analysis) is a formal document that attests to Iron (II) Phosphate's compliance with Iron (II) Phosphate specifications and serves as a tool for batch-level quality control.
Iron (II) Phosphate CoA mostly includes findings from lab analyses of a specific batch. For each Iron (II) Phosphate 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 (II) Phosphate may be tested according to a variety of international standards, such as European Pharmacopoeia (Iron (II) Phosphate EP), Iron (II) Phosphate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Iron (II) Phosphate USP).