Regulatory PathRegulatory requirements compared

Active substances

Ferrous sulfate + Folic acid

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
FERRO-FOL CAPSULE150,0.5 mg,mgCapsule · Oral use30 BlisterSAR 8.40Generic · OTCEIPICOValid
FOLICRON SR CAPSULE150,0.5 mg,mgSustained-release tablet · Oral use30 BlisterSAR 7.00Generic · OTCGulf Pharmaceutical Industries (Julphar)Valid
FEFOL SPANSULES150,0.5 mg,mgCapsule · Oral use30 BlisterSAR 8.60Generic · OTCMEDA ABWithdrawn by MAH · Not Marketed
FEFOL SPANSULES150, 0.5 mgCapsule · Oral use30 BlisterSAR 8.60Generic · OTCI.C.N.PHARMACEUTICALSWithdrawn by MAH · Not Marketed
FERAL CAPS150, 0.5 mgCapsule · Oral use30 BlisterSAR 7.25Generic · OTCHikma Pharmaceuticals PLCWithdrawn by MAH · Not Marketed
FERROGRAD-FOLIC TAB325, 350 mgTablet · Oral use30 BlisterSAR 9.10NCE · OTCAbbott LaboratoriesWithdrawn by MAH · Not Marketed
Indications — CHI Daman Drug Formulary

BARIATRIC SURGERY; IRON DEFICIENCY ANEMIA; MATERNAL AND CHILD HEALTHCARE- SUPPLEMENTATION FOR MOTHER AND CHILD

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

ProductStrengthForm · routeApplicantStatusFirst approved
FOLVRON182MG;0.33MGcapsule · oralLEDERLEDiscontinued13 Aug 1946

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
NHS Drug TariffFerrous sulfate 325mg / Folic acid 350microgram modified-release tablets£2.6430 tablet1 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.

Components

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.