Endo Inc. Announces Launch of FDA-Approved ADRENALIN® 8 mg/250 mL Premixed Bag, Expanding Ready-to-Use Epinephrine Line

Reuters
May 16, 2025
Endo Inc. Announces Launch of FDA-Approved ADRENALIN® 8 mg/250 mL Premixed Bag, Expanding Ready-to-Use Epinephrine Line

Endo Inc. has announced the launch of its new ADRENALIN® (epinephrine in 0.9% sodium chloride injection) 8 mg/250 mL premixed bag, which is the first FDA-approved and currently the only commercially available manufacturer-prepared epinephrine premixed IV bag. The product, which will begin shipping the week of May 19, 2025, aims to support healthcare providers by reducing complexity and streamlining operations in hospitals through its ready-to-use format. Endo Inc. also plans to offer additional concentrations in the future, expanding their TruDelivery® portfolio. No grant or funding from multiple organizations was mentioned in this announcement.

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. Endo Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: PH89493) on May 15, 2025, and is solely responsible for the information contained therein.

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