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Gland Pharma Secures USFDA Approval for Latanoprostene Bunod Ophthalmic Solution

Gland Pharma Secures USFDA Approval for Latanoprostene Bunod Ophthalmic Solution

Gland Pharma Ltd., a generic injectable and ophthalmic-focused pharmaceutical company, has received approval from the United States Food and Drug Administration (USFDA) for its Abbreviated New Drug Application for Latanoprostene Bunod Ophthalmic Solution, 0.024 percent.

The product is bioequivalent and therapeutically equivalent to the reference listed drug (RLD), VYZULTA Ophthalmic solution, 0.024 percent, of Bausch and Lomb, Inc.

This Product is indicated for the reduction of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension.

Gland Pharma is the exclusive first-to-file and is eligible for 180 days of generic drug exclusivity.

According to IQVIA, the product had US sales of approximately USD 171 million for the twelve months ending February 2025.

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More news about: global pharma | Published by Manvi | May - 01 - 2025 | 128

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