Glaucoma
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Sign up freeTop drugs studied for this disease
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FDA approval · 2026-04-09FDA Approved: COSOPT PF — Supplemental Application (Thea Pharma Inc.)
The FDA approved a supplemental application for COSOPT PF (dorzolamide hydrochloride and timolol maleate) by Thea Pharma Inc., marking an ad…
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FDA approval · 2026-04-02FDA Approved: ACETAZOLAMIDE — Supplemental Application (Lifestar Pharma LLC)
FDA approved a supplemental application for acetazolamide filed by Lifestar Pharma LLC under the ANDA program. The document does not specify…
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FDA approval · 2026-03-18FDA Approved: IOPIDINE 1% — Supplemental Application (Harrow Eye, LLC)
FDA approved a supplemental application for IOPIDINE 1% (apraclonidine hydrochloride ophthalmic solution) from Harrow Eye, LLC, indicating a…
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FDA approval · 2026-03-17FDA Approved: COMBIGAN — Supplemental Application (Allergan, Inc.)
FDA approved a supplemental application for COMBIGAN (brimonidine tartrate and timolol maleate) submitted by Allergan, Inc.
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FDA approval · 2026-02-25FDA Approved: TAFLUPROST OPHTHALMIC — Supplemental Application (Prasco Laboratories)
FDA approved a supplemental application for tafluprost ophthalmic from Prasco Laboratories, enabling the marketing of a generic tafluprost o…
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FDA approval · 2026-02-09FDA Approved: METHAZOLAMIDE — Original Application (Ajanta Pharma USA Inc.)
FDA approves Ajanta Pharma USA Inc.'s methazolamide under an Original Application (ANDA) for a generic glaucoma treatment.
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EMA approval · 2026-02-05EMA Authorised: DuoTrav (travoprost;timolol) — Novartis Europharm Limited
The EMA authorised DuoTrav, a fixed-dose combination eye drop of travoprost and timolol by Novartis Europharm Limited, for open-angle glauco…
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FDA approval · 2026-01-28FDA Approved: YUVEZZI — Original Application (Visus Therapeutics, Inc.)
The FDA approved YUVEZZI, a fixed-dose combination ophthalmic preparation of carbachol and brimonidine tartrate, under an original NDA from …
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FDA approval · 2026-01-27FDA Approved: IDOSE TR — Supplemental Application (Glaukos Corporation)
FDA approved a supplemental application for IDOSE TR, a travoprost intracameral product from Glaukos Corporation.
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EMA approval · 2026-01-23EMA Authorised: Travatan (travoprost) — Novartis Europharm Limited
EU marketing authorisation granted for Travatan eye drops (travoprost) by Novartis Europharm Limited for glaucoma (open-angle) and ocular hy…
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FDA approval · 2026-01-12FDA Approved: ACETAZOLAMIDE — Supplemental Application (Ajanta Pharma USA Inc.)
FDA approved Ajanta Pharma USA Inc.'s supplemental application for acetazolamide. This action approves changes to the product associated wit…
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FDA approval · 2025-11-21FDA Approved: BRIMONIDINE TARTRATE — Supplemental Application (Sandoz Inc)
FDA approved a supplemental application for BRIMONIDINE TARTRATE submitted by Sandoz Inc.
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FDA approval · 2025-10-09FDA Approved: TRAVATAN Z — Supplemental Application (Novartis Pharmaceuticals Corporation)
The FDA approved a supplemental application for TRAVATAN Z (travoprost) submitted by Novartis Pharmaceuticals Corporation, resulting in chan…
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FDA approval · 2025-10-01FDA Approved: DORZOLAMIDE HYDROCHLORIDE OPHTHALMIC SOLUTION — Supplemental Application (Micro Labs Limited)
FDA approved a supplemental application for dorzolamide hydrochloride ophthalmic solution from Micro Labs Limited.
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FDA approval · 2025-09-18FDA Approved: ALPHAGAN P — Supplemental Application (Allergan, Inc.)
The FDA approved a supplemental application for Alphagan P (brimonidine tartrate) submitted by Allergan, Inc.
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FDA approval · 2025-07-31FDA Approved: VIZZ — Original Application (LENZ Therapeutics, Inc.)
FDA approved VIZZ (aceclidine) from LENZ Therapeutics in an original new drug application.
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FDA approval · 2025-06-17FDA Approved: ACETAZOLAMIDE — Original Application (Sagent Pharmaceuticals)
FDA approved Sagent Pharmaceuticals' Original Application for Acetazolamide, including Acetazolamide and Acetazolamide Sodium formulations.
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FDA approval · 2025-05-30FDA Approved: ACETAZOLAMIDE — Original Application (Aurobindo Pharma Limited)
FDA approved Aurobindo Pharma Limited's original application for a generic acetazolamide product.
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FDA approval · 2025-05-27FDA Approved: DORZOLAMIDE AND TIMOLOL — Supplemental Application (Leading Pharma, LLC)
FDA approval of a supplemental application for the dorzolamide and timolol combination ophthalmic solution from Leading Pharma, LLC.
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FDA approval · 2025-05-20FDA Approved: TIMOLOL MALEATE — Supplemental Application (Rising Pharma Holdings, Inc.)
FDA approved a supplemental application for timolol maleate from Rising Pharma Holdings, Inc., authorizing changes to an existing generic pr…
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FDA approval · 2025-05-16FDA Approved: TIMOLOL MALEATE — Supplemental Application (First Nation Group, LLC)
The FDA approved a supplemental application for TIMOLOL MALEATE from First Nation Group, LLC, authorizing a new generic product on the marke…
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FDA approval · 2025-04-28FDA Approved: PILOCARPINE HYDROCHLORIDE OPHTHALMIC — Original Application (Amneal Pharmaceuticals NY LLC)
The FDA approved the original application for Pilocarpine Hydrochloride Ophthalmic from Amneal Pharmaceuticals NY LLC, providing a generic p…
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FDA approval · 2025-04-25FDA Approved: DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE — Supplemental Application (Gland Pharma Limited)
FDA approved a supplemental application for a generic dorzolamide hydrochloride and timolol maleate eye drop from Gland Pharma Limited. The …
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FDA approval · 2025-03-27FDA Approved: DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE OPHTHALMIC SOLUTION — Supplemental Application (Micro Labs Limited)
FDA approved a supplemental application from Micro Labs Limited for dorzolamide hydrochloride and timolol maleate ophthalmic solution. This …
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FDA approval · 2025-03-17FDA Approved: BIMATOPROST — Original Application (Lifestar Pharma LLC)
FDA approved the original application for Bimatoprost by Lifestar Pharma LLC, granting approval for a generic ophthalmic solution intended t…