Regulatory PathRegulatory requirements compared

Active substance

Diclofenac diethylamine

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
Avotrene Emulgel1 %Gel · Topical50 TubeSAR 7.20Generic · OTCMiddle East Pharmaceutical Industries Co Ltd Avalon PharmaValid
DICLOGESIC1 %Gel · Topical1 TubeSAR 7.80Generic · OTCDAR ALDAWAValid
RUMAFEN 1% gel1 %Gel · Topical1 TubeSAR 24.70Generic · OTCRIYADH PHARMAValid
VOLTAREN EMULGEL 1%1 %Gel · Topical1 TubeSAR 26.00NCE · OTCHaleon Schweiz AGValid
VOLTAREN EMULGEL 1%1 %Gel · Topical1 TubeSAR 17.05NCE · OTCHaleon Schweiz AGValid
Voltaren12 hours Emulgel2.32 %Gel · Topical1 TubeSAR 58.50NCE · OTCHaleon Schweiz AGValid
LOCAGEL1 %Gel · Topical1 TubeSAR 4.40Generic · OTCHAYAT PHARMACEUTICAL INDUSTRIESWithdrawn by MAH · Not Marketed
RUMAFEN 1% gel1 %Gel · Topical1 TubeSAR 7.05Generic · OTCRIYADH PHARMAWithdrawn by MAH · Not Marketed
Indications — CHI Daman Drug Formulary

LOW BACK PAIN; OSTEOARTHRITIS; PAIN MANAGEMENT IN CANCER PATIENTS; POSTOPERATIVE PAIN

Canada Canada — marketed products (Health Canada)

BrandDINStrengthForm · routeCompany
VOLTAREN EMULGEL ACTIVE025548011.16 % / W/WGEL · TOPICALHALEON CANADA ULC
VOLTAREN EMULGEL BACK & MUSCLE PAIN024650351.16 % / W/WGEL · TOPICALHALEON CANADA ULC
VOLTAREN EMULGEL EXTRA STRENGTH023931902.32 % / W/WGEL · TOPICALHALEON CANADA ULC
VOLTAREN EMULGEL JOINT PAIN EXTRA STRENGTH024650432.32 % / W/WGEL · TOPICALHALEON CANADA ULC
VOLTAREN EMULGEL JOINT PAIN REGULAR STRENGTH023385801.16 % / W/WGEL · TOPICALHALEON CANADA ULC

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.