Regulatory PathRegulatory requirements compared

Active substance

Potassium iodide

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
TERODA130 mgTablet · Oral use10 BlisterSAR 17.10Generic · PrescriptionSPIMACOValid
TERODA65 mgTablet · Oral use10 BlisterSAR 8.55Generic · PrescriptionSPIMACO ADDWAEIHValid
TERODA65 mgTablet · Oral use100 BlisterSAR 85.50Generic · PrescriptionSPIMACOValid
TERODA130 mgTablet · Oral use100 BlisterSAR 171.00Generic · PrescriptionSPIMACOValid
Indications — CHI Daman Drug Formulary

HYPERTHYROIDISM

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

ProductStrengthForm · routeApplicantStatusFirst approved
IOSAT130MG; 65MGtablet · oralANBEXOver-the-counter14 Oct 1982
THYROSAFE65MG; 130MGtablet · oralBTG INTLOver-the-counter10 Sep 2002
POTASSIUM IODIDE65MG/MLsolution · oralMISSION PHARMACALOver-the-counter24 Mar 2016
THYRO-BLOCK130MGtablet · oralMEDA PHARMSDiscontinued9 Nov 1979
POTASSIUM IODIDE1GM/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**solution · oralROXANEDiscontinued19 Feb 1982
THYROSHIELD65MG/MLsolution · oralARCO PHARMS LLCDiscontinued12 Jan 2005

WHO WHO Model List of Essential Medicines (2025)

  • 18.7. Thyroid hormones and antithyroid medicines · core (EML); complementary (EMLc)
    Thyrotoxicosis
    Oral > Solid > tablet: 65 mg (scored)
  • 6.3. Antifungal medicines · complementary
    Sporotrichosis
    Local > Topical > Solution: Saturated solution

Combinations containing Potassium iodide

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.