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    Chemistry

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    Also known as: Iron(3+);oxygen(2-);hydroxide, Ferric oxy-hydroxide, Ferric hydroxide [mi], Dtxsid3042057, Ferric oxyhydroxide (feo2h), Ferric hydroxide oxide (feooh)
    Molecular Formula
    FeHO2
    Molecular Weight
    88.85  g/mol
    InChI Key
    IEECXTSVVFWGSE-UHFFFAOYSA-M
    FDA UNII
    87PZU03K0K
    Iron Sucrose
    An antiferromagnetic material; constitutes the core of natural ferritin.
    Ferric oxyhydroxide is a Phosphate Binder. The mechanism of action of ferric oxyhydroxide is as a Phosphate Chelating Activity.
    1 2D Structure

    Iron Sucrose

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    iron(3+);oxygen(2-);hydroxide
    2.1.2 InChI
    InChI=1S/Fe.H2O.O/h;1H2;/q+3;;-2/p-1
    2.1.3 InChI Key
    IEECXTSVVFWGSE-UHFFFAOYSA-M
    2.1.4 Canonical SMILES
    [OH-].[O-2].[Fe+3]
    2.2 Other Identifiers
    2.2.1 UNII
    87PZU03K0K
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. 5fe2o3.9h2o

    2. Ferric Hydroxide Oxide

    3. Ferric Hydroxide Oxide (feooh)

    4. Ferric Oxy-hydroxide

    5. Ferric Oxyhydroxide (feo2h)

    6. Ferrihydrite

    7. Iron(iii) Oxyhydroxide

    2.3.2 Depositor-Supplied Synonyms

    1. Iron(3+);oxygen(2-);hydroxide

    2. Ferric Oxy-hydroxide

    3. Ferric Hydroxide [mi]

    4. Dtxsid3042057

    5. Ferric Oxyhydroxide (feo2h)

    6. Ferric Hydroxide Oxide (feooh)

    7. Db14695

    2.3.3 Other Synonyms

    1. Feojectin

    2. Ferplex Ss

    3. Ferrivenin

    4. Iviron

    5. Proferrin

    6. Sucrofer

    7. Iron Sugar

    8. Saccharated Iron

    9. Venoferrum

    10. Fesin

    11. Ferrum Vitis

    12. Hippiron

    13. Ferum Hausmann

    2.4 Create Date
    2006-10-25
    3 Chemical and Physical Properties
    Molecular Weight 88.85 g/mol
    Molecular Formula FeHO2
    Hydrogen Bond Donor Count1
    Hydrogen Bond Acceptor Count2
    Rotatable Bond Count0
    Exact Mass88.932590 g/mol
    Monoisotopic Mass88.932590 g/mol
    Topological Polar Surface Area2 Ų
    Heavy Atom Count3
    Formal Charge0
    Complexity0
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count3
    4 Drug and Medication Information
    4.1 Drug Information
    1 of 2  
    Drug NameVelphoro
    PubMed HealthSucroferric Oxyhydroxide (By mouth)
    Drug ClassesPhosphate Binder
    Active IngredientSucroferric oxyhydroxide
    Dosage FormTablet, chewable
    RouteOral
    Strength500mg
    Market StatusPrescription
    CompanyVifor Fresenius

    2 of 2  
    Drug NameVelphoro
    PubMed HealthSucroferric Oxyhydroxide (By mouth)
    Drug ClassesPhosphate Binder
    Active IngredientSucroferric oxyhydroxide
    Dosage FormTablet, chewable
    RouteOral
    Strength500mg
    Market StatusPrescription
    CompanyVifor Fresenius

    5 Pharmacology and Biochemistry
    5.1 FDA Pharmacological Classification
    5.1.1 Active Moiety
    FERRIC OXYHYDROXIDE
    5.1.2 FDA UNII
    87PZU03K0K
    5.1.3 Pharmacological Classes
    Mechanisms of Action [MoA] - Phosphate Chelating Activity

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    04-Mar-2021
    02-Apr-2025
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    ABOUT THIS PAGE

    Looking for 20344-49-4 / Sucroferric Oxyhydroxide API manufacturers, exporters & distributors?

    Sucroferric Oxyhydroxide manufacturers, exporters & distributors 1

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    PharmaCompass offers a list of Sucroferric Oxyhydroxide 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 Sucroferric Oxyhydroxide manufacturer or Sucroferric Oxyhydroxide supplier for your needs.

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    PharmaCompass also assists you with knowing the Sucroferric Oxyhydroxide API Price utilized in the formulation of products. Sucroferric Oxyhydroxide API Price is not always fixed or binding as the Sucroferric Oxyhydroxide Price is obtained through a variety of data sources. The Sucroferric Oxyhydroxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

    API | Excipient name

    Sucroferric Oxyhydroxide

    Synonyms

    Iron hydroxide oxide, Iron(3+);oxygen(2-);hydroxide, Iron hydroxide oxide nanoparticles / nanopowder, Iron oxide hydroxide, Iron hydroxide nanorods, Ferric oxy-hydroxide

    Cas Number

    20344-49-4

    Unique Ingredient Identifier (UNII)

    87PZU03K0K

    About Sucroferric Oxyhydroxide

    An antiferromagnetic material; constitutes the core of natural ferritin.

    Sucrofer Manufacturers

    A Sucrofer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sucrofer, including repackagers and relabelers. The FDA regulates Sucrofer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sucrofer API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

    click here to find a list of Sucrofer manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

    Sucrofer Suppliers

    A Sucrofer supplier is an individual or a company that provides Sucrofer active pharmaceutical ingredient (API) or Sucrofer finished formulations upon request. The Sucrofer suppliers may include Sucrofer API manufacturers, exporters, distributors and traders.

    click here to find a list of Sucrofer suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

    Sucrofer USDMF

    A Sucrofer DMF (Drug Master File) is a document detailing the whole manufacturing process of Sucrofer active pharmaceutical ingredient (API) in detail. Different forms of Sucrofer DMFs exist exist since differing nations have different regulations, such as Sucrofer USDMF, ASMF (EDMF), JDMF, CDMF, etc.

    A Sucrofer DMF submitted to regulatory agencies in the US is known as a USDMF. Sucrofer USDMF includes data on Sucrofer's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sucrofer USDMF is kept confidential to protect the manufacturer’s intellectual property.

    click here to find a list of Sucrofer suppliers with USDMF on PharmaCompass.

    Sucrofer KDMF

    In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

    Pharmaceutical companies submit a Sucrofer Drug Master File in Korea (Sucrofer KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sucrofer. The MFDS reviews the Sucrofer KDMF as part of the drug registration process and uses the information provided in the Sucrofer KDMF to evaluate the safety and efficacy of the drug.

    After submitting a Sucrofer KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Sucrofer API can apply through the Korea Drug Master File (KDMF).

    click here to find a list of Sucrofer suppliers with KDMF on PharmaCompass.

    Sucrofer WC

    A Sucrofer written confirmation (Sucrofer WC) is an official document issued by a regulatory agency to a Sucrofer manufacturer, verifying that the manufacturing facility of a Sucrofer active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sucrofer APIs or Sucrofer finished pharmaceutical products to another nation, regulatory agencies frequently require a Sucrofer WC (written confirmation) as part of the regulatory process.

    click here to find a list of Sucrofer suppliers with Written Confirmation (WC) on PharmaCompass.

    Sucrofer NDC

    National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Sucrofer as an active pharmaceutical ingredient (API).

    Finished drug products

    The FDA updates the NDC directory daily. The NDC numbers for Sucrofer API and other APIs are published in this directory by the FDA.

    Unfinished drugs

    The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

    Pharmaceutical companies that manufacture Sucrofer as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

    Compounded drug products

    The NDC directory also contains data on finished compounded human drug products that contain Sucrofer and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sucrofer NDC to their finished compounded human drug products, they may choose to do so.

    click here to find a list of Sucrofer suppliers with NDC on PharmaCompass.

    Sucrofer GMP

    Sucrofer 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 Sucrofer 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 Sucrofer GMP manufacturer or Sucrofer GMP API supplier for your needs.

    Sucrofer CoA

    A Sucrofer CoA (Certificate of Analysis) is a formal document that attests to Sucrofer's compliance with Sucrofer specifications and serves as a tool for batch-level quality control.

    Sucrofer CoA mostly includes findings from lab analyses of a specific batch. For each Sucrofer 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.

    Sucrofer may be tested according to a variety of international standards, such as European Pharmacopoeia (Sucrofer EP), Sucrofer JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sucrofer USP).

    Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
    For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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