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Heron Therapeutics' Zynrelef Vial Access Needle Receives FDA Approval

By RTTNews Staff Writer   ✉  | Published:  | Google News Follow Us  | Join Us
rttnewslogo20mar2024

Wednesday, Heron Therapeutics Inc. (HRTX) announced that the FDA has approved the Prior Approval Supplement Application for the Zynrelef Vial Access Needle or VAN. Following this announcement, the stock is up 4% in pre-market trading.

The VAN is designed to streamline aseptic preparation while cutting withdrawal time to between 20 and 45 seconds. This new design replaces the existing vented vial spike with a more user-friendly, container-like option, which could lead to safer usage, greater adoption, and improved preparation efficiency.

The company anticipates the VAN's release in the fourth quarter of 2024.

In pre-market activity on the Nasdaq, the shares are trading at $2.04, up 4.12%.

For comments and feedback contact: editorial@rttnews.com

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