Is Brompheniramine + Pseudoephedrine registered with the SFDA?

The SFDA human drug list (edition 4-2026, as published by the Council of Health Insurance) lists 0 valid registrations of Brompheniramine + Pseudoephedrine.

Is Brompheniramine + Pseudoephedrine approved by the US FDA?

Drugs@FDA lists 1 application product line for Brompheniramine + Pseudoephedrine, including EFIDAC 24 PSEUDOEPHEDRINE HYDROCHLORIDE/BROMPHENIRAMINE MALEATE (Discontinued).

Active substances

Brompheniramine + Pseudoephedrine

SFDA 1
US FDA 1

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade name	Strength	Form · route	Pack	Public price	Type	Company	Status
DIMETAPP ELIXIR ALCOHOL FREE	1, 15 mg/ml	Syrup · Oral use	1 Bottle	SAR 6.15	NCE · OTC	FEREVA RICHMOND	Withdrawn by MAH · Not Marketed

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

Product	Strength	Form · route	Applicant	Status	First approved
EFIDAC 24 PSEUDOEPHEDRINE HYDROCHLORIDE/BROMPHENIRAMINE MALEATE	16MG;240MG	tablet, extended release · oral	ALZA	Discontinued	29 Mar 1996

Components

Pseudoephedrine

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.