Amneal Pharmaceuticals Inc. Receives FDA Approval for Brekiya® Autoinjector for Acute Migraine and Cluster Headache Treatment

Reuters
2025/05/15
Amneal Pharmaceuticals Inc. Receives FDA Approval for Brekiya® Autoinjector for Acute Migraine and Cluster Headache Treatment

BRIDGEWATER, N.J., May 15, 2025 (GLOBE NEWSWIRE) -- Amneal Pharmaceuticals, Inc. (Nasdaq: AMRX) announced that it has received approval from the U.S. Food and Drug Administration (FDA) for Brekiya® (dihydroergotamine mesylate) injection. This marks the introduction of the first and only DHE autoinjector designed for the acute treatment of migraine with or without aura and cluster headaches in adults. The innovative autoinjector allows patients to self-administer the medication, traditionally used in hospitals, in a ready-to-use form. Brekiya will be available for appropriate patients in the second half of 2025, providing a convenient option for those seeking quick relief from these debilitating conditions without needing to visit an emergency room.

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: GNW9451945-en) on May 15, 2025, and is solely responsible for the information contained therein.

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