Regulatory PathRegulatory requirements compared

Active substance

Iron dextran

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
COSMOFER 625MG-2ML AMPOULES312.5 mg/mlSolution for injection/infusion · Intravenous use5 AmpouleSAR 88.90Generic · PrescriptionPHARMACOSMOS A/SValid
Indications — CHI Daman Drug Formulary

ADULT ACUTE MYELOID LEUKAEMIA (AML); ANEMIA IN CHRONIC KIDNEY DISEASE; CHRONIC KIDNEY DISEASE ASSOCIATED ANEMIA; MATERNAL AND CHILD HEALTHCARE- SUPPLEMENTATION FOR MOTHER AND CHILD

US FDA United States — FDA approvals (Drugs@FDA)

ProductStrengthForm · routeApplicantStatusFirst approved
INFEDEQ 100MG IRON/2ML (EQ 50MG IRON/ML)injectable · injectionALLERGANPrescription29 Apr 1974
IRON DEXTRANEQ 50MG IRON/MLinjectable · injectionSANOFI AVENTIS USDiscontinued25 Apr 1957
PROFERDEXEQ 50MG IRON/MLinjectable · injectionNEW RIVERDiscontinued26 Mar 1981
DEXFERRUMEQ 50MG IRON/MLinjectable · injectionAM REGENTDiscontinued23 Feb 1996

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
US NADACINFED 100 MG/2 ML VIAL$18.88981per ML23 Sep 2026
NHS Drug TariffIron dextran 100mg/2ml solution for injection ampoules£39.855 ampoule1 Oct 2026
NHS Drug TariffIron dextran 500mg/10ml solution for injection ampoules£79.702 ampoule1 Oct 2026

NADAC: average price US retail pharmacies pay to buy the medicine. NHS Drug Tariff Part VIIIA: basic price reimbursed to pharmacies in England and Wales.

Safety signals and safety-related labeling changes

All safety entries for iron dextran →

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.