SFDA Saudi Arabia — SFDA human drug list
| Trade name | Strength | Form · route | Pack | Public price | Type | Company | Status |
| SIMBRINZA DROPS SUSP | 2,10 mg/ml,mg/ml | Eye drops, suspension · Ocular use | 1 Dropper Container | SAR 64.60 | NCE · Prescription | NOVARTIS PHARMA AG | Valid |
Indications — CHI Daman Drug Formulary
OPEN ANGLE GLUCOMA
US FDA United States — FDA approvals (Drugs@FDA)
| Product | Strength | Form · route | Applicant | Status | First approved |
| SIMBRINZA | 0.2%;1% | suspension/drops · ophthalmic | ALCON LABS INC | Prescription | 19 Apr 2013 |
EMA European Union — centrally authorised medicines
Simbrinza Novartis Europharm Limited · Authorised · authorised 18 Jul 2014 · ATC S01EC54
Therapeutic indication (EMA)
Decrease of elevated intraocular pressure (IOP) in adult patients with open-angle glaucoma or ocular hypertension for whom monotherapy provides insufficient IOP reduction.
Canada Canada — marketed products (Health Canada)
| Brand | DIN | Strength | Form · route | Company |
| SIMBRINZA | 02435411 | 1 % / W/V; 0.2 % / W/V | SUSPENSION · OPHTHALMIC | NOVARTIS PHARMACEUTICALS CANADA INC |
Prices — United States and England
| Source | Product as listed | Price | Unit / pack | Date |
| US NADAC | SIMBRINZA 1%-0.2% EYE DROP | $26.03918 | per ML | 23 Sep 2026 |
| NHS Drug Tariff | Brinzolamide 10mg/ml / Brimonidine 2mg/ml eye drops | £9.23 | 5 ml | 1 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.
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.