Regulatory PathRegulatory requirements compared

Active substances

Diphtheria + Pertussis + Tetanus

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
D.T.COQ/D.T.P. VACCINE30, 60, 4 IUSuspension · Intramuscular use10 VialSAR 110.25Biological · PrescriptionSANOFI PASTEURWithdrawn by MAH · Not Marketed
D.T.Coq VACCINESuspension for injection · Intramuscular use20 AmpouleSAR 69.00Biological · PrescriptionSANOFI PASTEURWithdrawn by MAH · Not Marketed
INFANRIX 0.5ML PREFILLED SYRINGESuspension for injection · Intramuscular use1 Injection SyringeSAR 67.35Biological · PrescriptionGLAXO SAUDI ARABIAWithdrawn by MAH · Not Marketed
INFANRIX 0.5ML PREFILLED SYRINGESuspension for injection · Intramuscular use1 Injection SyringeSAR 67.35Biological · PrescriptionGLAXOSMITHKLINE (GSK)Withdrawn by MAH · Not Marketed
INFANRIX-HIB 0.5 ML SYRINGEPowder and suspension for suspension for injection · Intramuscular use1 Injection SyringeSAR 108.65Biological · PrescriptionGLAXO SAUDI ARABIAWithdrawn by MAH · Not Marketed
INFANRIX-HIB 0.5 ML SYRINGEPowder and suspension for suspension for injection · Intramuscular use1 Injection SyringeSAR 108.65Biological · PrescriptionGLAXOSMITHKLINE (GSK)Withdrawn by MAH · Not Marketed
TETRAMUNE VACCINESolution for injection · Intramuscular use1 VialSAR 632.70Biological · PrescriptionWYETHWithdrawn by MAH · Not Marketed
TRITANRIX-HB 10ug-ML 0.5ML VIALSolution · Intramuscular use1 VialSAR 42.65Biological · PrescriptionGLAXOSMITHKLINE (GSK)Withdrawn by MAH · Not Marketed

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.