VYZULTA Οphthalmic solution Ref.[10112] Active ingredients: Latanoprostene bunod

Source: FDA, National Drug Code (US)  Revision Year: 2019 

1. Indications and Usage

VYZULTA (latanoprostene bunod ophthalmic solution) 0.024% is indicated for the reduction of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension.

2. Dosage and Administration

The recommended dosage is one drop in the conjunctival sac of the affected eye(s) once daily in the evening. Do not administer VYZULTA (latanoprostene bunod ophthalmic solution), 0.024% more than once daily since it has been shown that more frequent administration of prostaglandin analogs may lessen the intraocular pressure lowering effect.

If VYZULTA is to be used concomitantly with other topical ophthalmic drug products to lower intraocular pressure, administer each drug product at least five (5) minutes apart.

16.2. Storage and Handling

Unopened bottle should be stored refrigerated at 2º to 8ºC (36º to 46ºF). Once a bottle is opened it may be stored at 2º to 25ºC (36º to 77ºF) for 8 weeks.

During shipment, bottles may be maintained at temperatures up to 40°C (104°F) for a period not exceeding 14 days.

Protect from light. Protect from freezing.

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