Amneal Pharmaceuticals Inc. has received U.S. Food and Drug Administration (FDA) approval for its cyclosporine ophthalmic emulsion 0.05%, a generic equivalent of RESTASIS®, for the treatment of dry eye disease. This sterile, preservative-free formulation is supplied in single-use vials and is indicated to increase tear production in patients with ocular inflammation-related dry eye syndrome. The product launch is expected in the first quarter of 2026.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Amneal Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9594606-en) on December 01, 2025, and is solely responsible for the information contained therein.
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