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MedsAcross

Fixed-dose combination

Brimonidine and Brinzolamide

Also known as brimonidine tartrate, brinzolamide
Available on requestOphthalmology
Presentations
1
Brands
1
Manufacturers
1
Available from stock
0

Brimonidine and Brinzolamide is a fixed-dose combination of a carbonic anhydrase inhibitor and an alpha-adrenergic agonist indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. MedsAcross supplies Brimonidine and Brinzolamide for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Alpha-Adrenergic Agonist, Carbonic Anhydrase Inhibitor, Adrenergic alpha-Agonists, Carbonic Anhydrase Inhibitors
ATC classification
S01EC54 Brimonidine and Brinzolamide · Eye medicines, subgroup S01E, subgroup S01EC
US FDA first approval
19 April 2013
EU status
Authorised
Orphan designation
No
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Ophthalmic
Dosage forms
Ophthalmic suspension
Fixed-dose combination of
Brimonidine, Brinzolamide
Identifiers
RxCUI 1421450Q48566822

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

SIMBRINZA (brinzolamide/brimonidine tartrate ophthalmic suspension) 1%/0.2% is a fixed combination of a carbonic anhydrase inhibitor and an alpha 2 adrenergic receptor agonist indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. SIMBRINZA is a combination of brinzolamide, a carbonic anhydrase inhibitor, and brimonidine tartrate, an alpha adrenergic agonist, indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension.

Source: US FDA prescribing information

How it works

SIMBRINZA is comprised of two components: brinzolamide (carbonic anhydrase inhibitor) and brimonidine tartrate (alpha 2 adrenergic receptor agonist). Each of these two components decreases elevated IOP. Elevated IOP is a major risk factor in the pathogenesis of optic nerve damage and glaucomatous visual field loss. The higher the level of IOP, the greater the likelihood of glaucomatous field loss and optic nerve damage. Brinzolamide inhibits carbonic anhydrase in the ciliary processes of the eye to decrease aqueous humor secretion, presumably by slowing the formation of bicarbonate ions with subsequent reduction in sodium and fluid transport. Brinzolamide has a peak ocular hypotensive effect occurring at 2 to 3 hours post-dosing.

Source: US FDA prescribing information

Dosing overview

The recommended dose is one drop of SIMBRINZA in the affected eye(s) three times daily. Shake well before use. SIMBRINZA ophthalmic suspension may be used concomitantly with other topical ophthalmic drug products to lower IOP. If more than one topical ophthalmic drug is being used, the drugs should be administered at least five minutes apart. Instill one drop in the affected eye(s) three times daily.

Source: US FDA prescribing information

Contraindications

Hypersensitivity to any component of this product. Neonates and infants (under the age of two years). Hypersensitivity SIMBRINZA is contraindicated in patients who are hypersensitive to any component of this product.

Source: US FDA prescribing information

Warnings and precautions

Potential for sulfonamide hypersensitivity reactions because of the brinzolamide component. Potential for corneal endothelium cell loss. Severe renal impairment may limit the metabolism of the brinzolamide component

Source: US FDA prescribing information

Side effects

Most common adverse reactions occurring in approximately 3% to 5% of patients included blurred vision, eye irritation, dysgeusia (bad taste), dry mouth, eye allergy.

Source: US FDA prescribing information

Interactions

Oral Carbonic Anhydrase Inhibitors. High-dose Salicylate Therapy. Central Nervous System Depressants. Antihypertensives/Cardiac Glycosides. Tricyclic Antidepressants. Monoamine Oxidase (MAO) Inhibitors

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

1 presentations of Brimonidine and Brinzolamide, sorted by availability.

MedicineActive ingredientManufacturerRegisterAvailability
Simbrinza 2 mg/10 mg per mL ophthalmic suspensionOphthalmicBrimonidine and BrinzolamideAlcon LaboratoriesUS FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 19 April 2013Drugs@FDA
EU (EMA)AuthorisedEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Questions and answers

Is Brimonidine and Brinzolamide available for export from India?

Yes, on request. MedsAcross lists 1 presentations of Brimonidine and Brinzolamide and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Brimonidine and Brinzolamide have?

The catalogue lists 1 brand names for Brimonidine and Brinzolamide, including Simbrinza.

Is Brimonidine and Brinzolamide approved by the US FDA?

Yes. The US FDA first approved Brimonidine and Brinzolamide on 19 April 2013, according to Drugs@FDA.

Is Brimonidine and Brinzolamide authorised in the European Union?

Yes. Brimonidine and Brinzolamide has a central EU marketing authorisation (status: authorised), according to European Medicines Agency data.

Does Brimonidine and Brinzolamide need cold chain shipping?

No listed presentation of Brimonidine and Brinzolamide is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

Which ATC class is Brimonidine and Brinzolamide in?

Brimonidine and Brinzolamide is classified under ATC code S01EC54 (Brimonidine and Brinzolamide).

References

  1. SIMBRINZA prescribing information (Alcon Laboratories). U.S. National Library of Medicine, DailyMed. Retrieved 11 March 2025
  2. Simbrinza: European public assessment report (EPAR). European Medicines Agency. Retrieved 23 January 2026

Request Brimonidine and Brinzolamide for export supply

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