Sucroferric Oxyhydroxide
Yes
No
Medical Assistance Fund
Active ingredients: Ferric Salts | Iron Salts
General information
Subsidy Information and Financing Scheme
[MAF] Sucroferric oxyhydroxide Chewable Tablet 500 mg
Treatment of hyperphosphataemia in patients with end-stage renal disease on haemodialysis or peritoneal dialysis who have persistent hyperphosphataemia despite optimising treatment with calcium-based phosphate binders, or who are unable to tolerate calcium-based phosphate binders due to hypercalcaemia.
Drug Guidance for Subsidy
The Ministry of Health’s Drug Advisory Committee has recommended:
Sucroferric oxyhydroxide 500 mg chewable tablet for treating hyperphosphataemia in patients with end-stage renal disease on haemodialysis or peritoneal dialysis who have persistent hyperphosphataemia despite optimising treatment with calcium-based phosphate binders, or who are unable to tolerate calcium-based phosphate binders due to hypercalcaemia.
Funding status
[R] Sucroferric oxyhydroxide 500 mg chewable tablet is recommended for inclusion on the Medication Assistance Fund (MAF) for the abovementioned indication from 1 November 2025.
General Availability in Public Healthcare Institution
Note:
General availability information reflected is based on the Public Healthcare Institutions’ (PHI) formulary on what is commonly used for treating their patient population and may or may not be available for patients not under the care of that institution. It does not reflect the PHI’s actual inventory availability and is subjected to change. Please consult the Public Hospitals or Polyclinics for details on availability and supply restrictions/considerations. General availability is not tied to any brand unless otherwise stated.
Users are to consult the respective PHIs for actual inventory availability and supply restrictions/consideration
Availability information
Formulation | Public Healthcare Institution |
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Chewable Tablet 500 mg |
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Registered Product(s) Information
Clinical and product info
Clinical info | Product Info |
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Information under the Indication, Dosage and Contraindication sections are extracted from the relevant Package Insert/Patient Information Leaflet of the product available on HSA Infosearch. For more information, please refer to the product's Package Insert/ Patient Information Leaflet available on HSA Infosearch. The information provided is for informational purposes only, and is not exhaustive. The information provided is not a substitute for professional medical advice. Please consult a qualified healthcare provider for any medical advice. | Information available here are product details as registered with the HSA. As this website is updated monthly, please refer to HSA Infosearch for the most updated product information. |
Oral
* Clinical information is available for this product.
